MUCAID

Catheters, Suction, Tracheobronchial

VYGON CORP.

The following data is part of a premarket notification filed by Vygon Corp. with the FDA for Mucaid.

Pre-market Notification Details

• Device ID: K910909
• 510k Number: K910909
• Device Name: MUCAID
• Classification: Catheters, Suction, Tracheobronchial
• Applicant: VYGON CORP. 227 BROADWAY SUITE 100 New York, NY 10007
• Contact: Harry A Schlakman
• Correspondent: Harry A Schlakman; VYGON CORP. 227 BROADWAY SUITE 100 New York, NY 10007
• Product Code: BSY
• CFR Regulation Number: 868.6810 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1991-03-05
• Decision Date: 1991-05-20