FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DADE INNOVIN

K Number: K974343 · Decision Jul 22, 1998
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
126
Applicant Total
30
Review Days
245

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Basic Information

Device Name
DADE INNOVIN
K Number
K974343
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.7750
Medical Specialty
Hematology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dade Intl., Inc.
Date Received
November 19, 1997
Decision Date
July 22, 1998
Product Code
GJS
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GJS Test, Time, Prothrombin

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GJS), ordered by most recent decision date.

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Other Clearances by Dade Intl., Inc.

K Number Device Name
K970505 DADE PFA-100 PLATELET FUNCTION ANALYZER/PFA COLLAGEN/EPINEPHRINE TEST CARTRIDGE/PFA COLLAGEN/ADP TEST CARTRIDGE/
K973974 DADE TRU-LIQUID CARDIAC CONTROL
K973668 CARDIAC TROPONIN-I (TROP) CALIBRATOR
K972524 DRIED GRAM-POSITIVE MIC/COMBO PANELS
K972782 DADE STRATUS CK-MB FLUOROMETRIC ENZYME IMMUNOASSAY
K972287 DADE TRU-LIQUID BILIRUBIN CONTROL
K964660 PARAMAX CHOLESTEROL REAGENT
K970676 DRIED GRAM-NEGATIVE MIC/COMBO PANELS
K964715 PARAMAX SALICYLATE REAGENT
K970330 DADE INDIRECT IMT SYSTEM WITH TCO2 ELECTRODE
Search all 30 clearances from Dade Intl., Inc. →