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FDA 510(k)

LOW-TOX-H RABBIT COMPLEMENT

K-Number: K790380 · 1979-03-21

Decision Date1979-03-21
Product CodeKTQ
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

LOW-TOX-H RABBIT COMPLEMENT is the device name listed in this FDA 510(k) record. The listed applicant is Cederlane Labs , Ltd.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790380. 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 LOW-TOX-H RABBIT COMPLEMENT?

LOW-TOX-H RABBIT COMPLEMENT is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Cederlane Labs , Ltd.. The 510(k) number is K790380.

When did LOW-TOX-H RABBIT COMPLEMENT receive FDA 510(k) clearance?

LOW-TOX-H RABBIT COMPLEMENT received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790380.

Who is the listed applicant for LOW-TOX-H RABBIT COMPLEMENT?

The FDA 510(k) record lists Cederlane Labs , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LOW-TOX-H RABBIT COMPLEMENT?

The FDA product code for LOW-TOX-H RABBIT COMPLEMENT is KTQ.

Related Clinical Trials

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.

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.

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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