Hamilton Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hamilton Co. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Hamilton Co. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1980 to 1996. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Hamilton Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hamilton Co.
16 devices
Cleared
Aug 16, 1996
MICROLAB 4000, MICROLAB 4200
Chemistry
92d
Cleared
Jan 30, 1995
DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER
Chemistry
195d
Cleared
Jun 02, 1989
MULTI-PROBE HEAD PLUS
Microbiology
57d
Cleared
Jan 05, 1988
LUMICON
Chemistry
104d
Cleared
May 29, 1987
MICROLAB AT
Microbiology
10d
Cleared
Aug 24, 1983
PB 600 REPEATING DISPENSER
Chemistry
48d
Cleared
Aug 24, 1983
MICROLAB P
Chemistry
48d
Cleared
Aug 24, 1983
PRECISION LIQUID DISPENSER
Chemistry
48d
Cleared
Aug 16, 1983
HC40/HC75 CATION EXCHANGE RESIN
Toxicology
40d
Cleared
Aug 16, 1983
PRP-1 REVERSED PHASE COLUMNS FOR HPLC
Toxicology
40d
Cleared
Aug 16, 1983
CHROM-PREP
Toxicology
40d
Cleared
Aug 12, 1983
PRP-1 REVERSED PHASE RESIN
Toxicology
36d