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FDA 510(k)

MODIFIED CPREVIVER

K-Number: K871147 · 1987-04-20

ApplicantAugerscope, Inc.
Decision Date1987-04-20
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED CPREVIVER is the device name listed in this FDA 510(k) record. The listed applicant is Augerscope, Inc.. It received FDA 510(k) clearance on 1987-04-20 under 510(k) number K871147. 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 MODIFIED CPREVIVER?

MODIFIED CPREVIVER is a medical device that received FDA 510(k) clearance on 1987-04-20. The listed applicant is Augerscope, Inc.. The 510(k) number is K871147.

When did MODIFIED CPREVIVER receive FDA 510(k) clearance?

MODIFIED CPREVIVER received FDA 510(k) clearance on 1987-04-20, under 510(k) number K871147.

Who is the listed applicant for MODIFIED CPREVIVER?

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

What is the FDA product code for MODIFIED CPREVIVER?

The FDA product code for MODIFIED CPREVIVER 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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Other records listing Augerscope, 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.

K864125CPREVIVER

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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