SABOURAUD LIQUID, BROTH MODIFIED
K-Number: K811326 · 1981-05-28
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Device Summary
Frequently Asked Questions
What is the SABOURAUD LIQUID, BROTH MODIFIED?
SABOURAUD LIQUID, BROTH MODIFIED is a medical device that received FDA 510(k) clearance on 1981-05-28. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811326.
When did SABOURAUD LIQUID, BROTH MODIFIED receive FDA 510(k) clearance?
SABOURAUD LIQUID, BROTH MODIFIED received FDA 510(k) clearance on 1981-05-28, under 510(k) number K811326.
Who is the listed applicant for SABOURAUD LIQUID, BROTH MODIFIED?
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 SABOURAUD LIQUID, BROTH MODIFIED?
The FDA product code for SABOURAUD LIQUID, BROTH MODIFIED is JSD.
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: JSD)
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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