ClearanceBrief
Company ยท US

Adri

FDA 510(k) clearances and medical device recalls filed under this name, 1987 to 2004. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
KMFBandage, Liquid2
FRODressing, Wound, Drug1
KGNWound Dressing With Animal-Derived Material(S)1
KHRAbsorber, Saliva, Paper1
MGQDressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 20, 2004K041268SILVERSITE OR CALGITROL
Adri
MGQ
Nov 15, 2002K011618CALGITROL AG SILVER ALGINATE WOUND DRESSING
Adri
FRO
Mar 13, 2000K000054FOAM CALCIUM ALGINATE TOPICAL WOUND DRESSING WITH COLLAGEN
Adri
KGN
Nov 12, 1996K963656FOAM CALCIUM ALIGINATE TOPICAL WOUND DRESSING
Adri
KMF
May 4, 1994K940404ALGINATE FIBER TOPICAL WOUND DRESSING
Adri
KMF
Apr 30, 1987K870383ALGINATE WOOL FIBER
Adri
KHR

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes