510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K980574Substantially Equivalent

Auraflex Tsh-3 200 Test Pack Model Number 80600, Auraflex Tsh-3 Calibrator Pack Model Number Number 80601 Auraflex Dil0

Alfa Biotech (Uk), Ltd., Aldershot, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K980574 is the FDA 510(k) clearance record for AURAFLEX TSH-3 200 TEST PACK MODEL NUMBER 80600, AURAFLEX TSH-3 CALIBRATOR PACK MODEL NUMBER NUMBER 80601 AURAFLEX DIL0, a class II device, cleared for Alfa Biotech (Uk) , Ltd. on under FDA product code JLW (Radioimmunoassay, Thyroid-Stimulating Hormone). FDA records list 3 510(k) clearances for Alfa Biotech (Uk) , Ltd., from to . As of , FDA records show no recalls naming K980574.

Clearance record

Decision date
Received
(35 days to decision)
Product code
JLW Radioimmunoassay, Thyroid-Stimulating Hormone
Regulation
21 CFR 862.1690
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Alfa Biotech (Uk) , Ltd. 4 Spring Lakes Estate,, Aldershot, GB
510(k) summary
Statement
Third party review
No

Clearances, product code JLW

Trailing 12 months
1 clearance under product code JLW in the twelve months to October 2026, February 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code JLW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20261
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260