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FDA 510(k)

APOLLO HEART RATE INDICATOR

K-Number: K791207 · 1979-08-28

Decision Date1979-08-28
Product CodeHCC
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

APOLLO HEART RATE INDICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Key Tronic Corp.. It received FDA 510(k) clearance on 1979-08-28 under 510(k) number K791207. The device is classified under product code HCC. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APOLLO HEART RATE INDICATOR?

APOLLO HEART RATE INDICATOR is a medical device that received FDA 510(k) clearance on 1979-08-28. The listed applicant is Key Tronic Corp.. The 510(k) number is K791207.

When did APOLLO HEART RATE INDICATOR receive FDA 510(k) clearance?

APOLLO HEART RATE INDICATOR received FDA 510(k) clearance on 1979-08-28, under 510(k) number K791207.

Who is the listed applicant for APOLLO HEART RATE INDICATOR?

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

What is the FDA product code for APOLLO HEART RATE INDICATOR?

The FDA product code for APOLLO HEART RATE INDICATOR is HCC.

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.

Related Devices (Code: HCC)

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

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