FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TEMPO2-I DISPOSABLE THERMOMETERS

K Number: K790890 · Decision Jun 27, 1979
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
13
Applicant Total
76
Review Days
51

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Basic Information

Device Name
TEMPO2-I DISPOSABLE THERMOMETERS
K Number
K790890
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.2900
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Airlife, Inc.
Date Received
May 7, 1979
Decision Date
June 27, 1979
Product Code
FQZ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FQZ Thermometer, Clinical Color Change

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Other Clearances by Airlife, Inc.

K Number Device Name
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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
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