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

DADE TRU-LIQUID CARDIAC CONTROL

K Number: K973974 · Decision Nov 6, 1997
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
96
Applicant Total
30
Review Days
17

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DADE TRU-LIQUID CARDIAC CONTROL
K Number
K973974
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dade Intl., Inc.
Date Received
October 20, 1997
Decision Date
November 6, 1997
Product Code
JJT
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
JJT Enzyme Controls (Assayed And Unassayed)

Similar 510(k) Clearances

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

View all

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/
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. →