COLUMBIA AGAR WITH 5% RABBIT BLOOD
K-Number: K780704 · 1978-05-12
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Device Summary
Frequently Asked Questions
What is the COLUMBIA AGAR WITH 5% RABBIT BLOOD?
COLUMBIA AGAR WITH 5% RABBIT BLOOD is a medical device that received FDA 510(k) clearance on 1978-05-12. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K780704.
When did COLUMBIA AGAR WITH 5% RABBIT BLOOD receive FDA 510(k) clearance?
COLUMBIA AGAR WITH 5% RABBIT BLOOD received FDA 510(k) clearance on 1978-05-12, under 510(k) number K780704.
Who is the listed applicant for COLUMBIA AGAR WITH 5% RABBIT BLOOD?
The FDA 510(k) record lists Granite Diagnostics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLUMBIA AGAR WITH 5% RABBIT BLOOD?
The FDA product code for COLUMBIA AGAR WITH 5% RABBIT BLOOD is JSI.
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.
Other records listing Granite Diagnostics, Inc. as applicant
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: JSI)
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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