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

AIR INCENTIVE SPIROMETER

K Number: K791819 · Decision Sep 26, 1979
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
107
Applicant Total
76
Review Days
12

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Basic Information

Device Name
AIR INCENTIVE SPIROMETER
K Number
K791819
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5690
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Airlife, Inc.
Date Received
September 14, 1979
Decision Date
September 26, 1979
Product Code
BWF
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
BWF Spirometer, Therapeutic (Incentive)

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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
K831246 WHISTLER IN-LINE PRESSURE RELEASE VALVE
K830895 SINGLE USE NEBULIZER, ADJUST. AIR-
K830896 HUMIDIFIER, WITH OR WITHOUT ADAPTER
K821129 AIRLIFE NEBULIZER HEATER
Search all 76 clearances from Airlife, Inc. →