DISPOSABLE STOPCOCKS

Stopcock, I.v. Set

PROCEDURE PRODUCTS, INC.

The following data is part of a premarket notification filed by Procedure Products, Inc. with the FDA for Disposable Stopcocks.

Pre-market Notification Details

• Device ID: K842173
• 510k Number: K842173
• Device Name: DISPOSABLE STOPCOCKS
• Classification: Stopcock, I.v. Set
• Applicant: PROCEDURE PRODUCTS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: FMG
• CFR Regulation Number: 880.5440 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1984-05-15
• Decision Date: 1984-09-05

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
B1608071F1	K842173	000