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FDA 510(k)

AIRWAY-CIRCULATION EVALUATOR

K-Number: K881483 · 1988-12-16

ApplicantResuscitation Ace, Inc.
Decision Date1988-12-16
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRWAY-CIRCULATION EVALUATOR is the device name listed in this FDA 510(k) record. The listed applicant is Resuscitation Ace, Inc.. It received FDA 510(k) clearance on 1988-12-16 under 510(k) number K881483. 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 AIRWAY-CIRCULATION EVALUATOR?

AIRWAY-CIRCULATION EVALUATOR is a medical device that received FDA 510(k) clearance on 1988-12-16. The listed applicant is Resuscitation Ace, Inc.. The 510(k) number is K881483.

When did AIRWAY-CIRCULATION EVALUATOR receive FDA 510(k) clearance?

AIRWAY-CIRCULATION EVALUATOR received FDA 510(k) clearance on 1988-12-16, under 510(k) number K881483.

Who is the listed applicant for AIRWAY-CIRCULATION EVALUATOR?

The FDA 510(k) record lists Resuscitation Ace, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRWAY-CIRCULATION EVALUATOR?

The FDA product code for AIRWAY-CIRCULATION EVALUATOR is BTM.

Related Clinical Trials

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.

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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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