Baker Instructions Corp. is one of 26109 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Baker Instructions Corp. - FDA 510(k) Cleared Devices
Recent clearances: SYSTEM 9000 DIFF MODEL AUTOMATED CELL COUNTER, BAKER TDM THEOPHYLLINE ASSAY, SYSTEM 9000 AUTOMATED CELL COUNTER
10
Total
10
Cleared
0
Denied
Baker Instructions Corp. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1981 to 1988. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Baker Instructions Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Baker Instructions Corp.
10 devices
Cleared
Sep 07, 1988
SYSTEM 9000 DIFF MODEL AUTOMATED CELL COUNTER
Hematology
75d
Cleared
Oct 20, 1987
BAKER TDM THEOPHYLLINE ASSAY
Toxicology
46d
Cleared
Mar 31, 1987
SYSTEM 9000 AUTOMATED CELL COUNTER
Hematology
48d
Cleared
Nov 04, 1985
UCD URINE SPECIMEN COLLECTOR
Gastroenterology & Urology
20d
Cleared
May 02, 1985
SYSTEM 8000 CELL COUNTER
Hematology
90d
Cleared
Nov 07, 1983
SPIRIT CHEMISTRY SYSTEM
Chemistry
55d
Cleared
Oct 04, 1983
ENCORE CHEMISTRY ANALYZER
Chemistry
53d
Cleared
Apr 05, 1983
ENCORE CHEMISTRY ANALYZER
Chemistry
35d
Cleared
Jul 30, 1982
HAEM-C PLUS BLOOD REFERENCE CONTROLS
Hematology
30d
Cleared
Jul 01, 1981
CENTRIFICHEM ALT/AGPT OPTIMIZED REAGENT
Chemistry
16d