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FDA 510(k)

MERCURY MEDICAL REUSABLE CPR BAG

K-Number: K970756 · 1997-10-31

ApplicantMercury Medical
Decision Date1997-10-31
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY MEDICAL REUSABLE CPR BAG is the device name listed in this FDA 510(k) record. The listed applicant is Mercury Medical. It received FDA 510(k) clearance on 1997-10-31 under 510(k) number K970756. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERCURY MEDICAL REUSABLE CPR BAG?

MERCURY MEDICAL REUSABLE CPR BAG is a medical device that received FDA 510(k) clearance on 1997-10-31. The listed applicant is Mercury Medical. The 510(k) number is K970756.

When did MERCURY MEDICAL REUSABLE CPR BAG receive FDA 510(k) clearance?

MERCURY MEDICAL REUSABLE CPR BAG received FDA 510(k) clearance on 1997-10-31, under 510(k) number K970756.

Who is the listed applicant for MERCURY MEDICAL REUSABLE CPR BAG?

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 MEDICAL REUSABLE CPR BAG?

The FDA product code for MERCURY MEDICAL REUSABLE CPR BAG is BTM.

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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.

K090710MERCURY CPAPK083056NEO-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 10-55370

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Related Devices (Code: BTM)

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.

K251631The BAG manual resuscitator and accessoriesLaerdal Medical ASK243861butterflyBVMCompact Medical, Inc.K221841EOlife®ArcheonK212905Sotair DeviceSafe Bvm CorporationK210288Disposable Manual ResuscitatorXiamen Compower Medical Tech. Co., Ltd.K181583Adult Single Use Resuscitator Bag without Pressure Relief, Adult Single Use Resuscitator Bag + Pressure Relief 40CMH20, Adult Single Use Resuscitator Bag + Pressure Relief 60CMH20, Pediatric Single Use Resuscitator Bag + Pressure Relief 40CMH20, Infant Single Use Resuscitator Bag + Pressure Relief 40CMH20Flexicare Medical 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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