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FDA 510(k)

OHMEDA PEEP VALVE FOR GMS ABSORBER

K-Number: K843835 · 1984-11-15

ApplicantOhmeda Medical
Decision Date1984-11-15
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHMEDA PEEP VALVE FOR GMS ABSORBER is the device name listed in this FDA 510(k) record. The listed applicant is Ohmeda Medical. It received FDA 510(k) clearance on 1984-11-15 under 510(k) number K843835. The device is classified under product code BYE. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHMEDA PEEP VALVE FOR GMS ABSORBER?

OHMEDA PEEP VALVE FOR GMS ABSORBER is a medical device that received FDA 510(k) clearance on 1984-11-15. The listed applicant is Ohmeda Medical. The 510(k) number is K843835.

When did OHMEDA PEEP VALVE FOR GMS ABSORBER receive FDA 510(k) clearance?

OHMEDA PEEP VALVE FOR GMS ABSORBER received FDA 510(k) clearance on 1984-11-15, under 510(k) number K843835.

Who is the listed applicant for OHMEDA PEEP VALVE FOR GMS ABSORBER?

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

What is the FDA product code for OHMEDA PEEP VALVE FOR GMS ABSORBER?

The FDA product code for OHMEDA PEEP VALVE FOR GMS ABSORBER is BYE.

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Other records listing Ohmeda Medical 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.

K123309GIRAFFE AND PANDA WARMERSK101788GIRAFFE OMNIBEDK101778GIRAFFE INCUBATORK090697MODIFICATION TO: GIRAFFE AND PANDA WARMERK072157MODIFICATION TO GIRAFFE AND PANDA WARMERS (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)K070377GIRAFFE AND PANDA WARMER

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Related Devices (Code: BYE)

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.

K160112Besmed PEEP ValveBesmed Health Business CorpK122610PLAXTRON CPAP SYSTEM, MODEL CH-FFM-87XX/CH-FFM-88XX SERIESSen MU Technology Co., Ltd.K112546O_TWO CPAP SYSTEMO-Two Medical Technologies, Inc.K110713WATERPAP VALVEAirways Development, LLCK103833NEOPIP PATIENT CIRCUIT WITH PEEPNeoforce Group, Inc.K092029VENTSTAR RESUSCITAIRE, MODEL MP00311, VENTSTAR RESUSCITAIRE CEU, MODEL MP00310Draeger Medical AG & Co. KG

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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