FDA 510(k)

PLATES FOR HUMAN C4 COMPLEMENT

K-Number: K772002 · 1977-11-02

Decision Date1977-11-02

Product CodeDBI

Advisory CommitteeIM

DecisionSubstantially Equivalent

Device Summary

PLATES FOR HUMAN C4 COMPLEMENT is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K772002. The device is classified under product code DBI. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLATES FOR HUMAN C4 COMPLEMENT?

PLATES FOR HUMAN C4 COMPLEMENT is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is G.D. Searle and Co.. The 510(k) number is K772002.

When did PLATES FOR HUMAN C4 COMPLEMENT receive FDA 510(k) clearance?

PLATES FOR HUMAN C4 COMPLEMENT received FDA 510(k) clearance on 1977-11-02, under 510(k) number K772002.

Who is the listed applicant for PLATES FOR HUMAN C4 COMPLEMENT?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLATES FOR HUMAN C4 COMPLEMENT?

The FDA product code for PLATES FOR HUMAN C4 COMPLEMENT is DBI.

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Related Devices (Code: DBI)

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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.