Alfa Biotech (Uk) , Ltd.

Alfa Biotech (Uk) , Ltd. holds 3 FDA 510(k) medical device clearances, cleared in 1998.

Top product codes for Alfa Biotech (Uk) , Ltd.

Recent clearances by Alfa Biotech (Uk) , Ltd.

K980574 — AURAFLEX TSH-3 200 TEST PACK MODEL NUMBER 80600, AURAFLEX TSH-3 CALIBRATOR PACK MODEL NUMBER NUMBER 80601 AURAFLEX DIL0Code JLW·1998-03-24
K974505 — AURAFLEX FERRITIN 200 TEST PACK 80500, AURAFLEX FERRITIN CALIBRATOR PACK 80501Code DBF·1998-02-17
K974027 — AURAFLEX FT3 150 TEST PACK, AURAFLEX FT3 CALIBRATOR PACKCode CDP·1998-02-02

Data sourced from openFDA. This site is unofficial and independent of the FDA.