FDA 510(k)

CUMEVAC

K-Number: K874410 · 1987-12-03

Decision Date1987-12-03

Product CodeFFD

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

CUMEVAC is the device name listed in this FDA 510(k) record. The listed applicant is Cumes-Honikman Partnership. It received FDA 510(k) clearance on 1987-12-03 under 510(k) number K874410. The device is classified under product code FFD. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUMEVAC?

CUMEVAC is a medical device that received FDA 510(k) clearance on 1987-12-03. The listed applicant is Cumes-Honikman Partnership. The 510(k) number is K874410.

When did CUMEVAC receive FDA 510(k) clearance?

CUMEVAC received FDA 510(k) clearance on 1987-12-03, under 510(k) number K874410.

Who is the listed applicant for CUMEVAC?

The FDA 510(k) record lists Cumes-Honikman Partnership as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CUMEVAC?

The FDA product code for CUMEVAC is FFD.

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Related Devices (Code: FFD)

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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.