Cleared Traditional

K862447 - PANCOAT T3 UPTAKE COATED TUBE RADIOIMMUNOASSAY KIT
(FDA 510(k) Clearance)

Oct 1986
Decision
102d
Days
Class 2
Risk

K862447 is an FDA 510(k) clearance for the PANCOAT T3 UPTAKE COATED TUBE RADIOIMMUNOASSAY KIT. This device is classified as a Radioassay, Triiodothyronine Uptake (Class II - Special Controls, product code KHQ).

Submitted by Pantex, Div. Bio-Analysis, Inc. (Santa Monica, US). The FDA issued a Cleared decision on October 7, 1986, 102 days after receiving the submission on June 27, 1986.

This device falls under the Chemistry FDA review panel. Regulated under 21 CFR 862.1715.

Submission Details

510(k) Number K862447 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 27, 1986
Decision Date October 07, 1986
Days to Decision 102 days
Submission Type Traditional
Review Panel Chemistry (CH)
Summary

Device Classification

Product Code KHQ — Radioassay, Triiodothyronine Uptake
Device Class Class II - Special Controls
CFR Regulation 21 CFR 862.1715

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