Fisher Scientific Co., LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Fisher Scientific Co., LLC - FDA 510(k) Cleared Devices
89
Total
89
Cleared
0
Denied
Fisher Scientific Co., LLC has 89 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 89 cleared submissions from 1976 to 1993. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Fisher Scientific Co., LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Fisher Scientific Co., LLC
89 devices
Cleared
Mar 23, 1993
MICROHEMATOCRIT ROTOR
Hematology
56d
Cleared
Mar 11, 1992
MARATHON 6K GENERAL-PURPOSE CENTRIFUGE
Hematology
72d
Cleared
Jan 08, 1992
MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE
Hematology
35d
Cleared
Mar 08, 1989
MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1
Chemistry
41d
Cleared
May 16, 1988
URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & II
Chemistry
52d
Cleared
Oct 20, 1987
FISHER DIAGNOSTICS HEMATALL III LAS REAGENT
Hematology
15d
Cleared
Sep 14, 1987
HISTOMATIC SLIDE STAINER, CODE-ON VERSION
Hematology
52d
Cleared
Apr 06, 1987
SERACHEM LIQUID SPINAL FLUID CONTROL (HUMAN)
Chemistry
20d
Cleared
Oct 29, 1986
HEMATALL-C PLUS HEMATOLOGY CONTROLS
Hematology
69d
Cleared
Jul 10, 1986
FISHER DIAGNOSTICS HEMATALL-C CALIBRATOR
Hematology
22d
Cleared
May 23, 1986
THERACHEM-PLUS, TRI-LEVEL TDC (TM)
Toxicology
53d
Cleared
Apr 11, 1986
THERACHEM, TDC THERAPEUTIC DRUG CONTROLS
Toxicology
31d
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