LOW-TOX-H RABBIT COMPLEMENT
K-Number: K790380 · 1979-03-21
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Device Summary
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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