Consolidated Medical Equipment, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Consolidated Medical Equipment, Inc. has 0 FDA recalls, 0 inspections, 15 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Consolidated Medical Equipment, Inc." is on file.

What these totals cover: FDA records filed under the name "Consolidated Medical Equipment, Inc." and its spelling variant "Consolidated Medical Equipment".

Latest 510(k)
Jan 9, 1986

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances15Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Reviewing Consolidated Medical Equipment, Inc. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Consolidated Medical Equipment, Inc. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Recent 510(k) clearances

15 510(k) clearances from Jan 29, 1980 to Jan 9, 1986.

K-NumberDeviceDate
K854040I.V. DRESSINGJan 9, 1986
K850132DISPOSABLE CONDUCTIVE ADHESIVE DIAGNOSTIC ECG ELECApr 9, 1985
K850130PRN ECG ELECTRODEApr 9, 1985
K850037CLOSED WOUND DRAINMar 19, 1985
K844942PLURA-GARD CHEST DRAINAGE SYSTEMMar 12, 1985
K850131CONDUCTIVE ADHESIVE POST-OP ELECTRODE-TENSMar 5, 1985
K850311DISPOS. CONDUCTIVE ADHESIVE TENS PADMar 5, 1985
K850133VENI-GARD AP & TPN, DERMA-SHIELD, DERMA-SHIELD JR.Feb 28, 1985
K850129MODIFIED CONDUCTIVE ADHESIVE ELECTROSURGICAL GROUNFeb 28, 1985
K844372HAND CONTROLLED ELECTROSURGICAL PENCIL DISPOSABLEFeb 21, 1985
K844371HAND CONTROLLED ELECTROSURGICAL PENCIL-REUSEABLEFeb 20, 1985
K820443SURGI-SCRAPEMar 8, 1982
K820082POST-OP ELECTRODE (TENS ELECTRODE)Jan 28, 1982
K802282ESOPHAGEAL ECG PREAMPLIFIER & SIGNAL CONOct 10, 1980
K800024I.V. TAPE DOWN HOLDERJan 29, 1980

Consolidated Medical Equipment, Inc. and the FDA: common questions

Has Consolidated Medical Equipment, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "Consolidated Medical Equipment, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Consolidated Medical Equipment, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "Consolidated Medical Equipment, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

Need more than this page shows? Ask about Consolidated Medical Equipment, Inc. in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.

Get a free API key

Prefer a PDF? Request a free supplier snapshot.

Is this your company or a supplier you list? Link to this FDA record from your site with a free button.

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.