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FDA 510(k)

F.R.C. APPARATUS

K-Number: K801088 · 1980-06-17

ApplicantHogan/Cologne Ent.
Decision Date1980-06-17
Product CodeBZC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

F.R.C. APPARATUS is the device name listed in this FDA 510(k) record. The listed applicant is Hogan/Cologne Ent.. It received FDA 510(k) clearance on 1980-06-17 under 510(k) number K801088. The device is classified under product code BZC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the F.R.C. APPARATUS?

F.R.C. APPARATUS is a medical device that received FDA 510(k) clearance on 1980-06-17. The listed applicant is Hogan/Cologne Ent.. The 510(k) number is K801088.

When did F.R.C. APPARATUS receive FDA 510(k) clearance?

F.R.C. APPARATUS received FDA 510(k) clearance on 1980-06-17, under 510(k) number K801088.

Who is the listed applicant for F.R.C. APPARATUS?

The FDA 510(k) record lists Hogan/Cologne Ent. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for F.R.C. APPARATUS?

The FDA product code for F.R.C. APPARATUS is BZC.

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Related Devices (Code: BZC)

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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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