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FDA 510(k)

RESUSCITATION TIMER, MODEL L770-CPR

K-Number: K073171 · 2008-01-31

ApplicantAllied Healthcare Products, Inc.
Decision Date2008-01-31
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RESUSCITATION TIMER, MODEL L770-CPR is the device name listed in this FDA 510(k) record. The listed applicant is Allied Healthcare Products, Inc.. It received FDA 510(k) clearance on 2008-01-31 under 510(k) number K073171. 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 RESUSCITATION TIMER, MODEL L770-CPR?

RESUSCITATION TIMER, MODEL L770-CPR is a medical device that received FDA 510(k) clearance on 2008-01-31. The listed applicant is Allied Healthcare Products, Inc.. The 510(k) number is K073171.

When did RESUSCITATION TIMER, MODEL L770-CPR receive FDA 510(k) clearance?

RESUSCITATION TIMER, MODEL L770-CPR received FDA 510(k) clearance on 2008-01-31, under 510(k) number K073171.

Who is the listed applicant for RESUSCITATION TIMER, MODEL L770-CPR?

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

What is the FDA product code for RESUSCITATION TIMER, MODEL L770-CPR?

The FDA product code for RESUSCITATION TIMER, MODEL L770-CPR is BTM.

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Related Devices (Code: BTM)

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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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