Simmler, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Simmler, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Simmler, Inc. has 23 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 23 cleared submissions from 1980 to 1989.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Simmler, Inc.
23 devices
Cleared
Nov 29, 1989
SICKLE CELL SOLUBILITY TEST KIT
Hematology
64d
Cleared
Feb 11, 1988
MULTICHEM(R) Y -GLUTAMYLTRANSFERASE (Y -GT)
Chemistry
72d
Cleared
Jan 21, 1988
MULTICHEM (R) MAGNESIUM REAGENT
Immunology
73d
Cleared
Jan 07, 1988
MULTICHEM HDL PRECIPITATING REAGENT #S0914
Chemistry
44d
Cleared
Dec 18, 1987
MULTICHEM CHLORIDE REAGENT S0933
Chemistry
24d
Cleared
Nov 25, 1987
MULTICHEM (R) TOTAL BILIRUBIN
Chemistry
36d
Cleared
Oct 29, 1987
MULTICHEM ALBUMIN REAGENT S0902
Chemistry
24d
Cleared
Oct 28, 1987
MULTICHEM INORGANIC PHOSPHOROUS S0923
Chemistry
23d
Cleared
Oct 20, 1987
MULTICHEM CREATININE REAGENT S0917
Chemistry
35d
Cleared
Oct 07, 1987
MULTICHEM ALKALINE PHOSPHATASE (S0903)
Chemistry
21d
Cleared
Oct 02, 1987
MULTICHEM CALCIUM S0910
Chemistry
18d
Cleared
Jun 11, 1987
MULTICHEM LDH-L REAGENT
Chemistry
16d