Medical Device Manufacturer · US , Mchenry , IL

Hamilton Co. - FDA 510(k) Cleared Devices

16 submissions · 16 cleared · Since 1980

Recent clearances: MICROLAB 4000, MICROLAB 4200, DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER

Total

Cleared

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.

Hamilton Co. is one of 14060 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Hamilton Co.

16 devices

1-12 of 16

Cleared Aug 16, 1996

MICROLAB 4000, MICROLAB 4200

K961896 · JQW

Chemistry · 92d

Cleared Jan 30, 1995

DISCRETE PHOTOMETRIC CHEMISTRY ANALYZER

K943493 · JJE

Chemistry · 195d

Cleared Jun 02, 1989

MULTI-PROBE HEAD PLUS

PB 600 REPEATING DISPENSER

PRECISION LIQUID DISPENSER

K832205 · JQW

Chemistry · 48d

Cleared Aug 16, 1983

HC40/HC75 CATION EXCHANGE RESIN

K832199 · DNH

Toxicology · 40d

Cleared Aug 16, 1983

PRP-1 REVERSED PHASE COLUMNS FOR HPLC

PRP-1 REVERSED PHASE RESIN

K832197 · DMZ

Toxicology · 36d

Hamilton Co. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Hamilton Co.

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