MULTIPLE

Dressing, Wound, Drug

DERMA-LOCK MEDICAL CORP.

The following data is part of a premarket notification filed by Derma-lock Medical Corp. with the FDA for Multiple.

Pre-market Notification Details

• Device ID: K831204
• 510k Number: K831204
• Device Name: MULTIPLE
• Classification: Dressing, Wound, Drug
• Applicant: DERMA-LOCK MEDICAL CORP. 4221 Richmond Rd., N.W. Walker, MI 49534
• Product Code: FRO
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-04-13
• Decision Date: 1983-11-28