OPEN END SPRING GUIDE

Wire, Guide, Catheter

C.R. BARD, INC.

The following data is part of a premarket notification filed by C.r. Bard, Inc. with the FDA for Open End Spring Guide.

Pre-market Notification Details

• Device ID: K832607
• 510k Number: K832607
• Device Name: OPEN END SPRING GUIDE
• Classification: Wire, Guide, Catheter
• Applicant: C.R. BARD, INC. 110 MARSHALL DRIVE Warrandale, PA 15086
• Product Code: DQX
• CFR Regulation Number: 870.1330 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1983-08-03
• Decision Date: 1983-12-27

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
20643169856664	K832607	000
20643169856657	K832607	000
20643169856640	K832607	000
20643169856633	K832607	000