CDC ANAEROBE BLOOD AGAR
K-Number: K854455 · 1985-11-18
Advertisement
Device Summary
Frequently Asked Questions
What is the CDC ANAEROBE BLOOD AGAR?
CDC ANAEROBE BLOOD AGAR is a medical device that received FDA 510(k) clearance on 1985-11-18. The listed applicant is R. Kent Richards, Inc.. The 510(k) number is K854455.
When did CDC ANAEROBE BLOOD AGAR receive FDA 510(k) clearance?
CDC ANAEROBE BLOOD AGAR received FDA 510(k) clearance on 1985-11-18, under 510(k) number K854455.
Who is the listed applicant for CDC ANAEROBE BLOOD AGAR?
The FDA 510(k) record lists R. Kent Richards, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CDC ANAEROBE BLOOD AGAR?
The FDA product code for CDC ANAEROBE BLOOD AGAR is JSG.
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 R. Kent Richards, 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: JSG)
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.
Advertisement