CONMED VENI-GARD(TM I.V. DRESSING-PRODUCT LINE EXTENSION AND MODIFICATIONS

Dressing, Wound And Burn, Occlusive

CONMED CORP.

The following data is part of a premarket notification filed by Conmed Corp. with the FDA for Conmed Veni-gard(tm I.v. Dressing-product Line Extension And Modifications.

Pre-market Notification Details

• Device ID: K950065
• 510k Number: K950065
• Device Name: CONMED VENI-GARD(TM I.V. DRESSING-PRODUCT LINE EXTENSION AND MODIFICATIONS
• Classification: Dressing, Wound And Burn, Occlusive
• Applicant: CONMED CORP. P.O. BOX 1408 Dayton, OH 45401 -1408
• Contact: Ira D Duesler, Jr.
• Correspondent: Ira D Duesler, Jr.; CONMED CORP. P.O. BOX 1408 Dayton, OH 45401 -1408
• Product Code: MGP
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-01-09
• Decision Date: 1995-03-24

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20653405014550	K950065	000