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

OXYGEN MONITOR OHIO 5100

K Number: K830446 · Decision Mar 24, 1983
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
120
Applicant Total
13
Review Days
42

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
OXYGEN MONITOR OHIO 5100
K Number
K830446
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1720
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Airco/Ohio Medical Products
Date Received
February 10, 1983
Decision Date
March 24, 1983
Product Code
CCL
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
CCL Analyzer, Gas, Oxygen, Gaseous-Phase

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CCL), ordered by most recent decision date.

View all

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
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 →