Browne Corp. FDA Record

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

Browne Corp. has 0 FDA recalls, 0 inspections, 7 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Browne Corp." is on file.

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

Latest 510(k)
Dec 6, 1979

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances7Nov 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

7 510(k) clearances from Jun 1, 1979 to Dec 6, 1979.

K-NumberDeviceDate
K792092BROWNE MODEL UD-4EDec 6, 1979
K792093BROWNE MODEL GD-5Dec 6, 1979
K792090BROWNE MODEL UD-4Dec 6, 1979
K792094BROWNE MODEL UA-6Dec 6, 1979
K792091BROWNE MODEL UD-4DDec 6, 1979
K790754BROWNE MODEL CF-1 AND CF-1GJun 1, 1979
K790478BROWNE MODEL UD-4DEJun 1, 1979

Browne Corp. and the FDA: common questions

Has Browne Corp. received an FDA warning letter?

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

FDA has not published a Form 483 for "Browne 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.