Hybritech, Inc. - FDA 510(k) Cleared Devices
63
Total
63
Cleared
0
Denied
FDA 510(k) Regulatory Record - Hybritech, Inc. Immunology ✕
6 devices
Cleared
Feb 17, 1993
TANDEM-E IGE II CALIBRATION VERIFICATION SET
Immunology
254d
Cleared
Nov 03, 1986
TANDEM-M IMMUNOENZYMETRIC ASSAY FOR IGE--
Immunology
31d
Cleared
Oct 08, 1986
TANDEM(R)-M FERRITIN IMMUNOENZYMETRIC ASSAY
Immunology
40d
Cleared
Aug 15, 1986
PHOTON ELITE/AUTOMATED RANDOM ACCESS IM/CH SYSTEM
Immunology
32d
Cleared
Oct 01, 1984
ENCORE IGE REAGENT
Immunology
31d
Cleared
Oct 19, 1981
FERRITIN KIT
Immunology
35d