510(k) K973806

DUODERM HYDROACTIVE GEL by Convatec, A Bristol-Myers Squibb Co. — Product Code MGQ

K973806 is an FDA 510(k) premarket notification submitted by Convatec, A Bristol-Myers Squibb Co. for the device "DUODERM HYDROACTIVE GEL". The FDA issued a decision of SN on December 29, 1997. The device falls under product code MGQ (Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic), a Class U device. Convatec, A Bristol-Myers Squibb Co. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
December 29, 1997
Date Received
October 6, 1997
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Dressing, Wound And Burn, Hydrogel W/Drug And/Or Biologic
Device Class
Class U
Regulation Number
Review Panel
SU
Submission Type