COMBIDERM ACD

Bandage, Liquid

CONVATEC, A BRISTOL-MYERS SQUIBB CO.

The following data is part of a premarket notification filed by Convatec, A Bristol-myers Squibb Co. with the FDA for Combiderm Acd.

Pre-market Notification Details

• Device ID: K954918
• 510k Number: K954918
• Device Name: COMBIDERM ACD
• Classification: Bandage, Liquid
• Applicant: CONVATEC, A BRISTOL-MYERS SQUIBB CO. P.O. BOX CN 5254 Princeton, NJ 08543 -5254
• Contact: Mcford Zamore
• Correspondent: Mcford Zamore; CONVATEC, A BRISTOL-MYERS SQUIBB CO. P.O. BOX CN 5254 Princeton, NJ 08543 -5254
• Product Code: KMF
• CFR Regulation Number: 880.5090 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-10-26
• Decision Date: 1995-12-26