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FDA 510(k)

DMR PLUS DISPOSABLE MANUAL RESUSCITATOR

K-Number: K973419 · 1998-03-25

ApplicantNellcor Puritan Bennett, Inc.
Decision Date1998-03-25
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DMR PLUS DISPOSABLE MANUAL RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Nellcor Puritan Bennett, Inc.. It received FDA 510(k) clearance on 1998-03-25 under 510(k) number K973419. 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 DMR PLUS DISPOSABLE MANUAL RESUSCITATOR?

DMR PLUS DISPOSABLE MANUAL RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1998-03-25. The listed applicant is Nellcor Puritan Bennett, Inc.. The 510(k) number is K973419.

When did DMR PLUS DISPOSABLE MANUAL RESUSCITATOR receive FDA 510(k) clearance?

DMR PLUS DISPOSABLE MANUAL RESUSCITATOR received FDA 510(k) clearance on 1998-03-25, under 510(k) number K973419.

Who is the listed applicant for DMR PLUS DISPOSABLE MANUAL RESUSCITATOR?

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

What is the FDA product code for DMR PLUS DISPOSABLE MANUAL RESUSCITATOR?

The FDA product code for DMR PLUS DISPOSABLE MANUAL RESUSCITATOR is BTM.

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Other records listing Nellcor Puritan Bennett, Inc. as applicant

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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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