ARGYLE CAROTID ARTERY LOOP SHUNT

Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

SHERWOOD MEDICAL CO.

The following data is part of a premarket notification filed by Sherwood Medical Co. with the FDA for Argyle Carotid Artery Loop Shunt.

Pre-market Notification Details

• Device ID: K822317
• 510k Number: K822317
• Device Name: ARGYLE CAROTID ARTERY LOOP SHUNT
• Classification: Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
• Applicant: SHERWOOD MEDICAL CO. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: DWF
• CFR Regulation Number: 870.4210 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1982-08-03
• Decision Date: 1982-08-31

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
00884521061036	K822317	000