DEOXYCHOLATE CITRATE AGAR
K-Number: K833204 · 1983-10-27
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Device Summary
Frequently Asked Questions
What is the DEOXYCHOLATE CITRATE AGAR?
DEOXYCHOLATE CITRATE AGAR is a medical device that received FDA 510(k) clearance on 1983-10-27. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K833204.
When did DEOXYCHOLATE CITRATE AGAR receive FDA 510(k) clearance?
DEOXYCHOLATE CITRATE AGAR received FDA 510(k) clearance on 1983-10-27, under 510(k) number K833204.
Who is the listed applicant for DEOXYCHOLATE CITRATE AGAR?
The FDA 510(k) record lists Acumedia Manufacturers, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DEOXYCHOLATE CITRATE AGAR?
The FDA product code for DEOXYCHOLATE CITRATE AGAR 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 Acumedia Manufacturers, 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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