Behring Diagnostics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Behring Diagnostics, Inc. - FDA 510(k) Cleared Devices
145
Total
145
Cleared
0
Denied
Behring Diagnostics, Inc. has 145 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 145 cleared submissions from 1976 to 1997.
Browse the FDA 510(k) cleared devices submitted by Behring Diagnostics, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Behring Diagnostics, Inc.
145 devices
Cleared
Oct 27, 1997
OPUS HLH CONTROLS
Toxicology
20d
Cleared
Oct 20, 1997
N ANTISERUM TO HUMAN ALBUMIN
Immunology
73d
Cleared
Oct 17, 1997
N ANTISERUM TO HUMAN TRANSFERRIN
Immunology
77d
Cleared
Sep 12, 1997
MODIFICATION OF OPUS FERRITIN TEST SYSTEM
Immunology
66d
Cleared
Sep 09, 1997
OPUS D-DIMER
Hematology
81d
Cleared
Jul 25, 1997
VON WILLEBRAND REAGENT
Hematology
50d
Cleared
Jul 22, 1997
OPUS ETHANOL
Toxicology
53d
Cleared
Jun 25, 1997
EMIT II OPIATES 300/2000 ASSAY
Toxicology
55d
Cleared
Jun 25, 1997
EMIT CALIBRATOR B LEVEL 1 (CUTOFF)/EMIT CALIBRATOR B LEVEL 2 (HIGH)
Toxicology
55d
Cleared
Jun 24, 1997
OPUS PSA TEST SYSTEM
Immunology
218d
Cleared
Jun 18, 1997
OPUS PROGESTERONE
Chemistry
40d
Cleared
May 19, 1997
BC THROMBIN REAGENT
Hematology
88d
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