FLUID THIOGLYCOLLATE MEDIUM
K-Number: K811047 · 1981-05-05
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Device Summary
Frequently Asked Questions
What is the FLUID THIOGLYCOLLATE MEDIUM?
FLUID THIOGLYCOLLATE MEDIUM is a medical device that received FDA 510(k) clearance on 1981-05-05. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811047.
When did FLUID THIOGLYCOLLATE MEDIUM receive FDA 510(k) clearance?
FLUID THIOGLYCOLLATE MEDIUM received FDA 510(k) clearance on 1981-05-05, under 510(k) number K811047.
Who is the listed applicant for FLUID THIOGLYCOLLATE MEDIUM?
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 FLUID THIOGLYCOLLATE MEDIUM?
The FDA product code for FLUID THIOGLYCOLLATE MEDIUM 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 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: 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.
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