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FDA 510(k)

OHIO TEMPERATURE SIMULATOR

K-Number: K832418 · 1983-09-12

ApplicantAirco/Ohio Medical Products
Decision Date1983-09-12
Product CodeFMZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

OHIO TEMPERATURE SIMULATOR 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 1983-09-12 under 510(k) number K832418. The device is classified under product code FMZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO TEMPERATURE SIMULATOR?

OHIO TEMPERATURE SIMULATOR is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Airco/Ohio Medical Products. The 510(k) number is K832418.

When did OHIO TEMPERATURE SIMULATOR receive FDA 510(k) clearance?

OHIO TEMPERATURE SIMULATOR received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832418.

Who is the listed applicant for OHIO TEMPERATURE SIMULATOR?

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 TEMPERATURE SIMULATOR?

The FDA product code for OHIO TEMPERATURE SIMULATOR is FMZ.

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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 ABSORBERK832565OHIO 5400 VOLUME MONITORK832185OHIO MODEL 922 SPIROMETERK830446OXYGEN MONITOR OHIO 5100K822456OHIO V5A ANESTHESIA VENTILATOR

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Related Devices (Code: FMZ)

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.

K260326Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)Datex-Ohmeda, Inc.K251619Babyleo TN500Drägerwerk AG & Co. KGaAK251663Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)Datex-Ohmeda, Inc.K243437mOm Essential Incubator (ME1)Mom Incubators LimitedK213553Giraffe Incubator Carestation CS1Datex Ohmeda, Inc.K190494Infant IncubatorNingbo David Medical Device Co., Ltd.

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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