THAYER MARTIN MEDIUM
K-Number: K841133 · 1984-03-23
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Device Summary
Frequently Asked Questions
What is the THAYER MARTIN MEDIUM?
THAYER MARTIN MEDIUM is a medical device that received FDA 510(k) clearance on 1984-03-23. The listed applicant is Anaerobe Systems. The 510(k) number is K841133.
When did THAYER MARTIN MEDIUM receive FDA 510(k) clearance?
THAYER MARTIN MEDIUM received FDA 510(k) clearance on 1984-03-23, under 510(k) number K841133.
Who is the listed applicant for THAYER MARTIN MEDIUM?
The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THAYER MARTIN MEDIUM?
The FDA product code for THAYER MARTIN MEDIUM is JSJ.
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 Anaerobe Systems 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: JSJ)
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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