Anatech, Ltd.

Anatech, Ltd. holds 14 FDA 510(k) medical device clearances, first cleared 1984, most recent 1988.

Top product codes for Anatech, Ltd.

Recent clearances by Anatech, Ltd.

K882873 — FIELDTEX HEMATOXYLINCode KQC·1988-07-28
K882874 — ZINC FORMALINCode LDX·1988-07-28
K882268 — ZINC FORMALIN CONCENTRATECode IGG·1988-06-15
K881282 — XYLENECode KEM·1988-04-05
K872663 — DRY-FORMCode IFP·1987-08-06
K872498 — HARRIS HEMATOXYLINCode HYK·1987-07-09
K872499 — ANATECH HEMATOXYLIN-NORMAL STRENGTHCode HYJ·1987-07-09
K872500 — ANATECH HEMATOXYLIN-EXTRA STRENGTHCode HYJ·1987-07-09
K870852 — NBF 10% NEUTRAL BUFFERED FORMALINCode IFP·1987-03-31
K842862 — CB FORMALINCode IGE·1984-08-28
K842940 — CBA FORMALINCode IFP·1984-08-28
K842861 — PRO-PAR CLEARANTCode KEM·1984-08-21
K842863 — PRO-SOFT DEHYDRANTCode PPM·1984-08-21
K842986 — REFRAX MOUNTING MEDIUMCode LEB·1984-08-21

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