ONE-WAY VALVE

Valve, Non-rebreathing

AIRLIFE, INC.

The following data is part of a premarket notification filed by Airlife, Inc. with the FDA for One-way Valve.

Pre-market Notification Details

• Device ID: K790151
• 510k Number: K790151
• Device Name: ONE-WAY VALVE
• Classification: Valve, Non-rebreathing
• Applicant: AIRLIFE, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050
• Product Code: CBP
• CFR Regulation Number: 868.5870 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1979-01-12
• Decision Date: 1979-03-12

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
30889483570566	K790151	000