Reliance Products Corp. FDA Record

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

Reliance Products Corp. has 0 FDA recalls, 0 inspections, 1 510(k) clearance and 0 compliance actions on record. No FDA warning letter addressed to "Reliance Products Corp." is on file.

What these totals cover: FDA records filed under the name "Reliance Products Corp." and its spelling variant "Reliance Products".

Latest 510(k)
Nov 21, 1983

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances1Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent 510(k) clearances

1 510(k) clearance on Nov 21, 1983.

K-NumberDeviceDate
K833450NUK BREAST SHIELDNov 21, 1983

Reliance Products Corp. and the FDA: common questions

Has Reliance Products Corp. received an FDA warning letter?

No FDA warning letter addressed to the name "Reliance Products Corp." 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 Reliance Products Corp. received an FDA Form 483?

FDA has not published a Form 483 for "Reliance Products Corp." in its reading room. FDA publishes some Form 483s, not all of them.

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