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FDA 510(k)

LIFE AID RESUSCITATOR

K-Number: K901218 · 1990-05-18

ApplicantClarendon Supplies , Ltd.
Decision Date1990-05-18
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIFE AID RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Clarendon Supplies , Ltd.. It received FDA 510(k) clearance on 1990-05-18 under 510(k) number K901218. 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 LIFE AID RESUSCITATOR?

LIFE AID RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1990-05-18. The listed applicant is Clarendon Supplies , Ltd.. The 510(k) number is K901218.

When did LIFE AID RESUSCITATOR receive FDA 510(k) clearance?

LIFE AID RESUSCITATOR received FDA 510(k) clearance on 1990-05-18, under 510(k) number K901218.

Who is the listed applicant for LIFE AID RESUSCITATOR?

The FDA 510(k) record lists Clarendon Supplies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFE AID RESUSCITATOR?

The FDA product code for LIFE AID RESUSCITATOR is BTM.

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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