510(k) K910553

Device
Roche Apolipoprotein Standard
Applicant
ROCHE DIAGNOSTIC SYSTEMS, INC.
510(k) number
K910553
Product code
DER
Decision
Substantially Equivalent (SESE)
Decision date
1991-05-08
Date received
1991-02-07
Regulation
866.5580
Classification name
Alpha-1-Lipoprotein, Antigen, Antiserum, Control
Medical specialty
Immunology
Review panel
Immunology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
CAROL L KRIEGER
Address
One Sunset Ave. Montclair NJ US 07042 07042

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code DER#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K013249TINA-QUANT APOLIPOPROTEIN VER.2Roche Diagnostics Corp.2001-11-16
K000921BAYER ADVIA IMS SYSTEM; 200 + 3Bayer Corp.2000-05-18
K993354K-ASSAY APO BKamiya Biomedical Co.1999-10-28
K993345K-ASSAY APO AIKamiya Biomedical Co.1999-10-25
K990594INTEGRA REAGENT CASSETTE FOR APOLIPOPROTEIN A-1Roche Diagnostics Corp.1999-04-14
K983289APOLIPOPROTEIN A1Abbott Laboratories1999-01-29
K964292N-ASSAY TIA APO A1 TEST KITCrestat Diagnostics, Inc.1997-08-01
K964294N-ASSAY TIA APO A1/B MULTI CALIBRATORCrestat Diagnostics, Inc.1997-08-01
K964296N-ASSAY TIA APO B TEST KITCrestat Diagnostics, Inc.1997-08-01
K904125UC IMU AEucardio Laboratory, Inc.1990-09-24
K872078QC3 WHOLE HUMAN SERUM, HDL-CHOLESTEROL CONTROLSolomon Park Research Laboratories1987-06-18
K854875APO-SCREEN CALIBRATOR & CONTROL SET FOR HDL APO A1Photec Diagnostics, Inc.1986-01-24
K853048APO-SCREEN TEST SET FOR HDL-APOLIPOPTEIN A-1Photec Diagnostics, Inc.1985-08-28
K851649APO A-I IMMUNOASSAY TEST SET FOR APOLIPOPROTEIN A1Photec Diagnostics, Inc.1985-06-05
K840830VENTRIA APO A-1 ALPHA-1 LIPOTROTEINVentrex Laboratories, Inc.1984-05-21