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FDA 510(k)

CPR PROMPT

K-Number: K853428 · 1985-09-06

ApplicantHutchins Tool & Engineering Co., Inc.
Decision Date1985-09-06
Product Code
DecisionSubstantially Equivalent

Device Summary

CPR PROMPT is the device name listed in this FDA 510(k) record. The listed applicant is Hutchins Tool & Engineering Co., Inc.. It received FDA 510(k) clearance on 1985-09-06 under 510(k) number K853428. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR PROMPT?

CPR PROMPT is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is Hutchins Tool & Engineering Co., Inc.. The 510(k) number is K853428.

When did CPR PROMPT receive FDA 510(k) clearance?

CPR PROMPT received FDA 510(k) clearance on 1985-09-06, under 510(k) number K853428.

Who is the listed applicant for CPR PROMPT?

The FDA 510(k) record lists Hutchins Tool & Engineering Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

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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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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