Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

C.P.R. COUNTING PACER

K-Number: K781636 · 1978-10-11

Decision Date1978-10-11
Product Code
DecisionSubstantially Equivalent

Device Summary

C.P.R. COUNTING PACER is the device name listed in this FDA 510(k) record. The listed applicant is Qual-Tec, Inc.. It received FDA 510(k) clearance on 1978-10-11 under 510(k) number K781636. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the C.P.R. COUNTING PACER?

C.P.R. COUNTING PACER is a medical device that received FDA 510(k) clearance on 1978-10-11. The listed applicant is Qual-Tec, Inc.. The 510(k) number is K781636.

When did C.P.R. COUNTING PACER receive FDA 510(k) clearance?

C.P.R. COUNTING PACER received FDA 510(k) clearance on 1978-10-11, under 510(k) number K781636.

Who is the listed applicant for C.P.R. COUNTING PACER?

The FDA 510(k) record lists Qual-Tec, 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.

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.

↑