VASCULAR CLAMP

Clamp, Vascular

TEXAS MEDICAL PRODUCTS, INC.

The following data is part of a premarket notification filed by Texas Medical Products, Inc. with the FDA for Vascular Clamp.

Pre-market Notification Details

• Device ID: K801395
• 510k Number: K801395
• Device Name: VASCULAR CLAMP
• Classification: Clamp, Vascular
• Applicant: TEXAS MEDICAL PRODUCTS, INC. 4221 Richmond Rd., N.W. Walker, MI 49534
• Product Code: DXC
• CFR Regulation Number: 870.4450 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1980-06-13
• Decision Date: 1980-06-30

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
B0662010030006	K801395	000
B066201003NS1	K801395	000