Fisher Scientific Co., LLC - FDA 510(k) Cleared Devices
Recent clearances: MICROHEMATOCRIT ROTOR, MARATHON 6K GENERAL-PURPOSE CENTRIFUGE, MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGE
89
Total
89
Cleared
0
Denied
FDA 510(k) Regulatory Record - Fisher Scientific Co., LLC Hematology ✕
16 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
Oct 20, 1987
FISHER DIAGNOSTICS HEMATALL III LAS REAGENT
Hematology
15d
Cleared
Sep 14, 1987
HISTOMATIC SLIDE STAINER, CODE-ON VERSION
Hematology
52d
Cleared
Oct 29, 1986
HEMATALL-C PLUS HEMATOLOGY CONTROLS
Hematology
69d
Cleared
Jul 10, 1986
FISHER DIAGNOSTICS HEMATALL-C CALIBRATOR
Hematology
22d
Cleared
Mar 24, 1983
MICROHEMATOCRIT READER
Hematology
29d
Cleared
Feb 01, 1983
HEMATOLOGY QUALITY CONTROL MIXTURE
Hematology
34d
Cleared
Jan 21, 1983
MICRO-HEMATOCRIT CENTRIFUGE 335/336
Hematology
50d
Cleared
Jun 24, 1982
REAGENT FOR COULTER COUNTER MODEL 5+11
Hematology
16d
Cleared
May 12, 1982
HEMATALL-C PLUS HEMATOLOGY CONTROLS
Hematology
56d
Cleared
Nov 05, 1979
FISHER DIAGNOSTICS HEMATOLOGY CONTROLS
Hematology
21d
Cleared
Apr 03, 1979
LISS REAGENT
Hematology
21d
Cleared
Apr 03, 1979
HEMATROL S HEMATOLOGY CONTROLS
Hematology
19d
Cleared
Oct 24, 1978
ALKALINE PHOSPHATASE IN SERUM
Hematology
35d