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Quali-Med, Inc.

FDA Regulatory Profile

Quali-Med, Inc. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Apr 27, 1987

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances7Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Qualimed
Same company group		0200—

Recent 510(k) Clearances

K-NumberDeviceDate
K871408BLOOD VESSEL CONNECTORApr 27, 1987
K862972DISPOSABLE MIRRORSep 23, 1986
K862472QUARTZ RODS TITANIUM RODSSep 12, 1986
K862241STANDARD BASIN KIT CUSTOM BASIN KITAug 1, 1986
K862242PAP SMEAR KITJun 26, 1986
K862172QUALI-MED'S OPERATING ROOM DRAPESJun 19, 1986
K861198CUSTOM PROCEDURE KIT (VARIOUS SUB-TITLES)May 16, 1986

FDA data resources