Cleared Traditional

K833193 - RADIOIMMUNOASSAY, THYROID STIMU. HORMONE
(FDA 510(k) Clearance)

Feb 1984
Decision
138d
Days
Class 2
Risk

K833193 is an FDA 510(k) clearance for the RADIOIMMUNOASSAY, THYROID STIMU. HORMONE. This device is classified as a Radioimmunoassay, Thyroid-stimulating Hormone (Class II - Special Controls, product code JLW).

Submitted by Biosan Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on February 4, 1984, 138 days after receiving the submission on September 19, 1983.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1690.

Submission Details

510(k) Number K833193 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received September 19, 1983
Decision Date February 04, 1984
Days to Decision 138 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code JLW — Radioimmunoassay, Thyroid-stimulating Hormone
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1690

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