Simmler, Inc.
Simmler, Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1989.
Top product codes for Simmler, Inc.
Recent clearances by Simmler, Inc.
- K895745 — SICKLE CELL SOLUBILITY TEST KIT
- K874903 — MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)
- K874595 — MULTICHEM (R) MAGNESIUM REAGENT
- K874820 — MULTICHEM HDL PRECIPITATING REAGENT #S0914
- K874812 — MULTICHEM CHLORIDE REAGENT S0933
- K874311 — MULTICHEM (R) TOTAL BILIRUBIN
- K874049 — MULTICHEM ALBUMIN REAGENT S0902
- K874038 — MULTICHEM INORGANIC PHOSPHOROUS S0923
- K873725 — MULTICHEM CREATININE REAGENT S0917
- K873761 — MULTICHEM ALKALINE PHOSPHATASE (S0903)
- K873697 — MULTICHEM CALCIUM S0910
- K872010 — MULTICHEM LDH-L REAGENT
- K871975 — MULTICHEM TOTAL PROTEIN REAGENT #S0928
- K871976 — MULTICHEM GLUCOSE HEXOKINASE REAGENT #S0919
- K853244 — TOTAL PROTEIN REAGENT FOR ASTRA 8 STAT/ROU ANALYZE
- K853049 — ALBUMIN REAGENT FOR ASTRA 8 AUTO STAT/ROUT ANALYZE
- K853050 — CALCIUM REAGENT FOR ASTRA 8 AUTOM STAT/ROUT/ANALYZ
- K843938 — LINEAR ENZYMATIC URIC ACID SYSTEM
- K831700 — MULTICHEM ENZYMATIC CHOLESTEROL SYS
- K831398 — LINEAR ENZMATIC URIC ACID SYSTEM
- K801222 — REAGENTS FOR ASTRA 8 AUTOMATED ANALYZER
- K800199 — LINEAR ENZYMATIC CHOLESTEROL SYSTEM
- K800200 — LINEAR ENZYMATIC GLUCOSE SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.