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FDA 510(k)

FECATEST

K-Number: K780564 · 1978-06-30

ApplicantOtto C. Watzka
Decision Date1978-06-30
Product CodeKHE
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

FECATEST is the device name listed in this FDA 510(k) record. The listed applicant is Otto C. Watzka. It received FDA 510(k) clearance on 1978-06-30 under 510(k) number K780564. The device is classified under product code KHE. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FECATEST?

FECATEST is a medical device that received FDA 510(k) clearance on 1978-06-30. The listed applicant is Otto C. Watzka. The 510(k) number is K780564.

When did FECATEST receive FDA 510(k) clearance?

FECATEST received FDA 510(k) clearance on 1978-06-30, under 510(k) number K780564.

Who is the listed applicant for FECATEST?

The FDA 510(k) record lists Otto C. Watzka as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FECATEST?

The FDA product code for FECATEST is KHE.

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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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