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FDA 510(k)

SAVE RESUSCITATOR

K-Number: K073410 · 2008-09-12

ApplicantArtivent Corporation
Decision Date2008-09-12
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SAVE RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Artivent Corporation. It received FDA 510(k) clearance on 2008-09-12 under 510(k) number K073410. 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 SAVE RESUSCITATOR?

SAVE RESUSCITATOR is a medical device that received FDA 510(k) clearance on 2008-09-12. The listed applicant is Artivent Corporation. The 510(k) number is K073410.

When did SAVE RESUSCITATOR receive FDA 510(k) clearance?

SAVE RESUSCITATOR received FDA 510(k) clearance on 2008-09-12, under 510(k) number K073410.

Who is the listed applicant for SAVE RESUSCITATOR?

The FDA 510(k) record lists Artivent Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAVE RESUSCITATOR?

The FDA product code for SAVE 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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