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

OHIO NON-REUSABLE TRACHEAL TUBE MAJILL

K Number: K812880 · Decision Nov 24, 1981
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
240
Applicant Total
13
Review Days
41

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Basic Information

Device Name
OHIO NON-REUSABLE TRACHEAL TUBE MAJILL
K Number
K812880
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5730
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Airco/Ohio Medical Products
Date Received
October 14, 1981
Decision Date
November 24, 1981
Product Code
BTR
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
BTR Tube, Tracheal (W/Wo Connector)

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Other Clearances by Airco/Ohio Medical Products

K Number Device Name
K833459 COAXIAL VOL. VENTILATOR CIRCUIT
K833452 OHIO GMS ABSORBER
K832418 OHIO TEMPERATURE SIMULATOR
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
K811413 DABC NONCONDUCTIVE PEDIAT. ANESTH. CIR
Search all 13 clearances from Airco/Ohio Medical Products →