THIOGLYCOLLATE GELATIN MEDIUM
K-Number: K811335 · 1981-05-29
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Device Summary
Frequently Asked Questions
What is the THIOGLYCOLLATE GELATIN MEDIUM?
THIOGLYCOLLATE GELATIN MEDIUM is a medical device that received FDA 510(k) clearance on 1981-05-29. The listed applicant is Acumedia Manufacturers, Inc.. The 510(k) number is K811335.
When did THIOGLYCOLLATE GELATIN MEDIUM receive FDA 510(k) clearance?
THIOGLYCOLLATE GELATIN MEDIUM received FDA 510(k) clearance on 1981-05-29, under 510(k) number K811335.
Who is the listed applicant for THIOGLYCOLLATE GELATIN 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 THIOGLYCOLLATE GELATIN MEDIUM?
The FDA product code for THIOGLYCOLLATE GELATIN MEDIUM is JSH.
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: JSH)
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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