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

OHIO TEMPERATURE SIMULATOR

K Number: K832418 · Decision Sep 12, 1983
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
84
Applicant Total
13
Review Days
52

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Basic Information

Device Name
OHIO TEMPERATURE SIMULATOR
K Number
K832418
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5400
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Airco/Ohio Medical Products
Date Received
July 22, 1983
Decision Date
September 12, 1983
Product Code
FMZ
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
FMZ Incubator, Neonatal

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Other Clearances by Airco/Ohio Medical Products

K Number Device Name
K833459 COAXIAL VOL. VENTILATOR CIRCUIT
K833452 OHIO GMS ABSORBER
K832565 OHIO 5400 VOLUME MONITOR
K832185 OHIO MODEL 922 SPIROMETER
K830446 OXYGEN MONITOR OHIO 5100
K822456 OHIO V5A ANESTHESIA VENTILATOR
K813476 OHIO VOLUME INCENTIVE SPIROMETER
K812879 OHIO NON-REUSABLE TRACHEAL TUBE MURPHY
K812880 OHIO NON-REUSABLE TRACHEAL TUBE MAJILL
K811413 DABC NONCONDUCTIVE PEDIAT. ANESTH. CIR
Search all 13 clearances from Airco/Ohio Medical Products →