FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

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K Number: K831246 · Decision Jul 26, 1983
Classifications
1
FEI Numbers
70
Registration Numbers
70
Same Product Code
102
Applicant Total
76
Review Days
99

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Basic Information

Device Name
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K Number
K831246
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5870
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Airlife, Inc.
Date Received
April 18, 1983
Decision Date
July 26, 1983
Product Code
CBP
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CBP Valve, Non-Rebreathing

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Other Clearances by Airlife, Inc.

K Number Device Name
K834573 AQUA TRAP
K834570 VOLUME VENTILATOR CIRCUIT W/WATER TRAP
K834077 SINGLE USE NEBULIZER-ADJUST-AIR ENTRAIN
K833196 VOLUME VENTILATOR CIRCUIT-NEBULIZER
K833197 TRACH SWIVE/CONNECTOR
K832725 DUAL DIAL VENTURI STYLE MASK
K830895 SINGLE USE NEBULIZER, ADJUST. AIR-
K830896 HUMIDIFIER, WITH OR WITHOUT ADAPTER
K821129 AIRLIFE NEBULIZER HEATER
K821128 DISPOSABLE THERMOPLASTIC RUBBER MOUTH
Search all 76 clearances from Airlife, Inc. →