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FDA 510(k)

MERCURY CPAP

K-Number: K090710 · 2009-08-20

ApplicantMercury Medical
Decision Date2009-08-20
Product CodeBYE
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY CPAP is the device name listed in this FDA 510(k) record. The listed applicant is Mercury Medical. It received FDA 510(k) clearance on 2009-08-20 under 510(k) number K090710. 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 MERCURY CPAP?

MERCURY CPAP is a medical device that received FDA 510(k) clearance on 2009-08-20. The listed applicant is Mercury Medical. The 510(k) number is K090710.

When did MERCURY CPAP receive FDA 510(k) clearance?

MERCURY CPAP received FDA 510(k) clearance on 2009-08-20, under 510(k) number K090710.

Who is the listed applicant for MERCURY CPAP?

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

What is the FDA product code for MERCURY CPAP?

The FDA product code for MERCURY CPAP is BYE.

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Other records listing Mercury 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.

K083056NEO-STAT CO2 <KGK032593MERCURY MEDICAL NEGATIVE INSPIRATORY FORCE (NIF) DISPOSABLE MONOMETERK031814STATCO2METER, MODEL 10-55372K031411MINI STATCO2 CO2 DETECTOR, MODEL 10-55371K021576MERCURY MEDICAL STATCO2 END TIDAL CO2 DETECTOR, MODEL 10-55370K001714MERCURY MEDICAL HYPERINFLATION BAG SYSTEM, MODEL 83-900-0149

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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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