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.
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
Looking for a specific device from Fisher Scientific Co., LLC? Search by device name or K-number.
Search all Fisher Scientific Co.,... devices