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FDA 510(k)

OHIO MODEL 922 SPIROMETER

K-Number: K832185 · 1983-08-12

ApplicantAirco/Ohio Medical Products
Decision Date1983-08-12
Product CodeBZG
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHIO MODEL 922 SPIROMETER is the device name listed in this FDA 510(k) record. The listed applicant is Airco/Ohio Medical Products. It received FDA 510(k) clearance on 1983-08-12 under 510(k) number K832185. The device is classified under product code BZG. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO MODEL 922 SPIROMETER?

OHIO MODEL 922 SPIROMETER is a medical device that received FDA 510(k) clearance on 1983-08-12. The listed applicant is Airco/Ohio Medical Products. The 510(k) number is K832185.

When did OHIO MODEL 922 SPIROMETER receive FDA 510(k) clearance?

OHIO MODEL 922 SPIROMETER received FDA 510(k) clearance on 1983-08-12, under 510(k) number K832185.

Who is the listed applicant for OHIO MODEL 922 SPIROMETER?

The FDA 510(k) record lists Airco/Ohio Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OHIO MODEL 922 SPIROMETER?

The FDA product code for OHIO MODEL 922 SPIROMETER is BZG.

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Other records listing Airco/Ohio Medical Products as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K833459COAXIAL VOL. VENTILATOR CIRCUITK833452OHIO GMS ABSORBERK832418OHIO TEMPERATURE SIMULATORK832565OHIO 5400 VOLUME MONITORK830446OXYGEN MONITOR OHIO 5100K822456OHIO V5A ANESTHESIA VENTILATOR

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Related Devices (Code: BZG)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251777MESI mTABLET SPIROMesi D.O.O.K241843TD-7301 Spirometer (TD-7301)Gostar Co., Ltd.K231416Air Next (NVD-02)Nuvoair ABK230501Spirobank OxiMir Medical International Research USAK230178EasyOne Sky SpirometerNdd Medizintechnik AGK222525Alveoair Digital SpirometerRoundworks Technologies Private Limited

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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