Hybritech, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hybritech, Inc. - FDA 510(k) Cleared Devices
63
Total
63
Cleared
0
Denied
Hybritech, Inc. has 63 FDA 510(k) cleared chemistry devices. Based in Mchenry, US.
Historical record: 63 cleared submissions from 1981 to 1997.
Browse the complete list of FDA 510(k) cleared chemistry devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Hybritech, Inc.
63 devices
Cleared
Sep 11, 1997
TANDEM-MP OSTASE IMMUNOENZYMETRIC ASSAY
Chemistry
57d
Cleared
Aug 19, 1996
TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
Chemistry
118d
Cleared
Jan 11, 1994
TANDEM-R OSTASE IMMUNORADIOMETRIC ASSAY
Chemistry
328d
Cleared
Feb 17, 1993
TANDEM-E IGE II CALIBRATION VERIFICATION SET
Immunology
254d
Cleared
Jul 30, 1992
HYBRITECH STRATUS PAP FLUOROMETRIC ENZYME IMMUNO
Chemistry
108d
Cleared
Jul 17, 1992
TANDEM-E HCG CALIBRATION VERIFICATION CONTROL SET
Chemistry
162d
Cleared
Jul 17, 1992
TANDEM-E FERRITIN CALIBRATION VERIFICATION CONROL
Chemistry
123d
Cleared
Jun 09, 1992
TANDEM ICON QSR CKMB IMMUNOENZYMETRIC ASSAY
Chemistry
56d
Cleared
Aug 28, 1991
TANDEM-E TSH CALIBRATION VERIFICATION CONTROL SET
Chemistry
86d
Cleared
Jul 24, 1991
ICON STREP B IMMUNOENZYMETRIC ASSAY
Microbiology
114d
Cleared
Oct 03, 1990
ICON STREP B IMMUNOENZYMETRIC ASSAY
Microbiology
86d
Cleared
Oct 31, 1989
TANDEM-E LH IMMUNOENZYMETRIC ASSAY KIT
Chemistry
78d
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