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FDA 510(k)

GUINEA PIG COMPLEMENT REGULAR

K-Number: K812370 · 1981-09-08

ApplicantDutchland Laboratories, Inc.
Decision Date1981-09-08
Product CodeKTQ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

GUINEA PIG COMPLEMENT REGULAR is the device name listed in this FDA 510(k) record. The listed applicant is Dutchland Laboratories, Inc.. It received FDA 510(k) clearance on 1981-09-08 under 510(k) number K812370. The device is classified under product code KTQ. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GUINEA PIG COMPLEMENT REGULAR?

GUINEA PIG COMPLEMENT REGULAR is a medical device that received FDA 510(k) clearance on 1981-09-08. The listed applicant is Dutchland Laboratories, Inc.. The 510(k) number is K812370.

When did GUINEA PIG COMPLEMENT REGULAR receive FDA 510(k) clearance?

GUINEA PIG COMPLEMENT REGULAR received FDA 510(k) clearance on 1981-09-08, under 510(k) number K812370.

Who is the listed applicant for GUINEA PIG COMPLEMENT REGULAR?

The FDA 510(k) record lists Dutchland Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GUINEA PIG COMPLEMENT REGULAR?

The FDA product code for GUINEA PIG COMPLEMENT REGULAR is KTQ.

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Related Devices (Code: KTQ)

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.

K890417SPQ(TM) ANTIBODY REAGENT SET II FOR C3Atlantic AntibodiesK812522RABBIT COMPLEMENTDutchland Laboratories, Inc.K812369GUINEA PIG COMPLEMENT VIRUS ANTIBODYDutchland Laboratories, Inc.K791117RABBIT COMPLEMENTCalbiochem-Behring Corp.K790380LOW-TOX-H RABBIT COMPLEMENTCederlane Labs , Ltd.

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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