510(k) K062751

Device
MODIFICATION TO QUANTIMETRIX CARDIASURE CARDIAC MARKER
Applicant
Quantimetrix Corp.
510(k) number
K062751
Product code
JJT
Decision
Substantially Equivalent (SESE)
Decision date
2006-10-03
Date received
2006-09-14
Regulation
862.1660
Classification name
Enzyme Controls (Assayed And Unassayed)
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Special
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
BERNICE NAVARRO
Address
2005 Manhattan Beach Blvd. Redondo Beach CA US 90278 90278

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JJT#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K984437QUANTEX ASO-CRP-RP CONTROL IIInstrumentation Laboratory CO1999-02-02
K984277CARDIOIMMUNE CARDIAC MARKER CONTROL LEVELS 1,2, AND 3Medical Analysis Systems, Inc.1998-12-09
K982845CARDIAC MARKERS CONTROL (SINGLE USE)-LEVELS, 1,2,3, MODELS NUMBER 175-1, 175-2, 175-3More Diagnostics1998-08-21
K980556LIQUICHEK CARDIAC MARKERS CONTROL LTBio-Rad1998-02-25
K974461TRIAGE CARDIAC CONTROLS, TRIAGE TROPONIN-I CONTROL, TRIAGE CK-MB CONTROL, TRIAGE MYOGLOBIN CONTROLBiosite Incorporated1997-12-10
K973974DADE TRU-LIQUID CARDIAC CONTROLDade Intl., Inc.1997-11-06
K972976CARDIAC MARKERS CONTROL - LEVEL 1, LEVEL 2, LEVEL 3, TRI-LEVELMore Diagnostics1997-08-29