AEROVENT

Connector, Airway (extension)

MONAGHAN MEDICAL CORP.

The following data is part of a premarket notification filed by Monaghan Medical Corp. with the FDA for Aerovent.

Pre-market Notification Details

• Device ID: K894969
• 510k Number: K894969
• Device Name: AEROVENT
• Classification: Connector, Airway (extension)
• Applicant: MONAGHAN MEDICAL CORP. FRANKLYN BLDG RT. 9 NORTH P.O. BOX 978 Plattsburgh, NY 12901
• Contact: James A Cochie
• Correspondent: James A Cochie; MONAGHAN MEDICAL CORP. FRANKLYN BLDG RT. 9 NORTH P.O. BOX 978 Plattsburgh, NY 12901
• Product Code: BZA
• CFR Regulation Number: 868.5810 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1989-08-07
• Decision Date: 1989-10-30