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

PARAMAX SALICYLATE REAGENT

K Number: K964715 · Decision Apr 25, 1997
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
28
Applicant Total
30
Review Days
151

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Basic Information

Device Name
PARAMAX SALICYLATE REAGENT
K Number
K964715
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3830
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dade Intl., Inc.
Date Received
November 25, 1996
Decision Date
April 25, 1997
Product Code
DKJ
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DKJ Colorimetry, Salicylate

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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
K970330 DADE INDIRECT IMT SYSTEM WITH TCO2 ELECTRODE
Search all 30 clearances from Dade Intl., Inc. →