AUTOSTAT ANTI-THYROID MICROSSOMAL
K-Number: K923371 · 1992-09-22
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Device Summary
Frequently Asked Questions
What is the AUTOSTAT ANTI-THYROID MICROSSOMAL?
AUTOSTAT ANTI-THYROID MICROSSOMAL is a medical device that received FDA 510(k) clearance on 1992-09-22. The listed applicant is Cogent Diagnotics , Ltd.. The 510(k) number is K923371.
When did AUTOSTAT ANTI-THYROID MICROSSOMAL receive FDA 510(k) clearance?
AUTOSTAT ANTI-THYROID MICROSSOMAL received FDA 510(k) clearance on 1992-09-22, under 510(k) number K923371.
Who is the listed applicant for AUTOSTAT ANTI-THYROID MICROSSOMAL?
The FDA 510(k) record lists Cogent Diagnotics , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOSTAT ANTI-THYROID MICROSSOMAL?
The FDA product code for AUTOSTAT ANTI-THYROID MICROSSOMAL is JNL.
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 Cogent Diagnotics , Ltd. 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: JNL)
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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