Dade Intl., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dade Intl., Inc. - FDA 510(k) Cleared Devices
30
Total
30
Cleared
0
Denied
Dade Intl., Inc. has 30 FDA 510(k) cleared medical devices. Based in Deerfield, US.
Historical record: 30 cleared submissions from 1995 to 1998. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Dade Intl., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dade Intl., Inc.
30 devices
Cleared
Jul 22, 1998
DADE INNOVIN
Hematology
245d
Cleared
Nov 17, 1997
DADE PFA-100 PLATELET FUNCTION ANALYZER/PFA COLLAGEN/EPINEPHRINE TEST...
Hematology
280d
Cleared
Nov 06, 1997
DADE TRU-LIQUID CARDIAC CONTROL
Chemistry
17d
Cleared
Oct 20, 1997
CARDIAC TROPONIN-I (TROP) CALIBRATOR
Chemistry
25d
Cleared
Sep 08, 1997
DRIED GRAM-POSITIVE MIC/COMBO PANELS
Microbiology
63d
Cleared
Aug 15, 1997
DADE STRATUS CK-MB FLUOROMETRIC ENZYME IMMUNOASSAY
Chemistry
21d
Cleared
Jul 07, 1997
DADE TRU-LIQUID BILIRUBIN CONTROL
Chemistry
18d
Cleared
Jun 04, 1997
PARAMAX CHOLESTEROL REAGENT
Chemistry
196d
Cleared
May 02, 1997
DRIED GRAM-NEGATIVE MIC/COMBO PANELS
Microbiology
67d
Cleared
Apr 25, 1997
PARAMAX SALICYLATE REAGENT
Toxicology
151d
Cleared
Apr 14, 1997
DADE INDIRECT IMT SYSTEM WITH TCO2 ELECTRODE
Chemistry
76d
Cleared
Mar 28, 1997
PARAMAX TRIGLYCERID REAGENT
Chemistry
148d