Autostat Anti-Thyroid Microssomal

FDA 510(k) K923371 · Cogent Diagnotics , Ltd.

Substantially Equivalent

510(k) numberK923371

Submission

Device name
Autostat Anti-Thyroid Microssomal
Applicant
Cogent Diagnotics , Ltd.
Dunblane, Fk15 9ep, GB
Received
July 9, 1992
Decision date
September 22, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
JNL – Immunochemical, Thyroglobulin Autoantibody
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5870
Specialty
Immunology

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Questions and answers

When was Autostat Anti-Thyroid Microssomal cleared by the FDA?

Autostat Anti-Thyroid Microssomal (K923371) received a 510(k) decision of Substantially Equivalent on September 22, 1992, 75 days after the submission was received.

What is the product code of K923371?

The FDA product code is JNL – Immunochemical, Thyroglobulin Autoantibody, a Class II (moderate risk) device regulated under 21 CFR 866.5870.