FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PARAMAX TRIGLYCERID REAGENT

K Number: K964346 · Decision Mar 28, 1997
Classifications
1
FEI Numbers
39
Registration Numbers
39
Same Product Code
150
Applicant Total
30
Review Days
148

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Basic Information

Device Name
PARAMAX TRIGLYCERID REAGENT
K Number
K964346
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1705
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dade Intl., Inc.
Date Received
October 31, 1996
Decision Date
March 28, 1997
Product Code
CDT
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CDT Lipase Hydrolysis/Glycerol Kinase Enzyme, Triglycerides

Similar 510(k) Clearances

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

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Other Clearances by Dade Intl., Inc.

K Number Device Name
K974343 DADE INNOVIN
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
Search all 30 clearances from Dade Intl., Inc. →