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FDA 510(k)

RESUSCITATOR

K-Number: K874567 · 1988-02-29

ApplicantAmerican Medical Technology, Inc.
Decision Date1988-02-29
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is American Medical Technology, Inc.. It received FDA 510(k) clearance on 1988-02-29 under 510(k) number K874567. 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 RESUSCITATOR?

RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1988-02-29. The listed applicant is American Medical Technology, Inc.. The 510(k) number is K874567.

When did RESUSCITATOR receive FDA 510(k) clearance?

RESUSCITATOR received FDA 510(k) clearance on 1988-02-29, under 510(k) number K874567.

Who is the listed applicant for RESUSCITATOR?

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

What is the FDA product code for RESUSCITATOR?

The FDA product code for RESUSCITATOR is BTM.

Related Clinical Trials

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Other records listing American Medical Technology, Inc. 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.

K963808CHOICE POWERED WHEELCHAIRK905745AMETEC MASY MODULAR ANGIOSCOPE SYSTEMK874430NEEDLE CONTAINERK874360PLASTIC TUBING CONNECTORK873313SURGICAL DRAPE

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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