510(k) K022519

Device
LDL CHOLESTEROL (AUTOMATED)
Applicant
Jas Diagnostics, Inc.
510(k) number
K022519
Product code
JHM
Decision
Substantially Equivalent (SESE)
Decision date
2002-09-30
Date received
2002-07-30
Regulation
862.1475
Classification name
Colorimetric Method, Lipoproteins
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
No

Applicant Contact#

Contact
David Johnston
Address
7220 NW 58th St. Miami FL US 33166 33166

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code JHM#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K120662PICCOLO HDL-CAPILLARY TEST SYSTEMAbaxis, Inc.2012-04-24
K081300DIMENSION VISTA HDLC FLEX REAGENT CARTRIDGESiemens Healthcare Diagnostics2008-07-02
K073072DIMENSION AHDL FLEX REAGENT CARTRIDGE, MODEL: DF48BDade Behring, Inc.2008-02-21
K032798DIMENSION AUTOMATED HDL CHOLESTEROL (AHDL) FLEX REAGENT CARTRIDGE (DF48A) CATALOG # DF48ADade Behring, Inc.2003-10-30
K983849DIMENSION AUTOMATED HIGH DENSITY LIPOPROTEIN CHOLESTEROL (ADHL) FLEX REAGENT CARTRIDGEDade Behring, Inc.1999-01-11
K902935ROCHE COBAS READY HDL CHOLESTEROL REAGENTRoche Diagnostic Systems, Inc.1990-09-27
K841056HDL PRECIPITANT REAGENT SETMedical Specialties, Inc.1984-05-01
K780173LYPOPROTEIN CHOLESTEROL TEST KITEnvironmental Chemical Specialties1978-05-03