FDA.reportPublic FDA data

510(k) K932989

Device
Coat-a-count Free Estriol
Applicant
DIAGNOSTIC PRODUCTS CORP.
510(k) number
K932989
Product code
CGI
Decision
Substantially Equivalent (SESE)
Decision date
1994-12-19
Date received
1993-06-18
Regulation
862.1265
Classification name
Radioimmunoassay, Estriol
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
KENNETH ASARCH
Address
5700 W. 96th St. Los Angeles CA US 90045 90045

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code CGI#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K974721UNCONJUGATED ESTRIOL ASSAY FOR THE BAYER IMMUNO 1 SYSTEM (IN VITRO DIAGNOSTIC SYSTEM)Bayer Corp.1998-03-03
K962875ACTIVE ULTRASENSITIVE UNCONJUGATED ESTRIOL EIADiagnostic Systems Laboratories, Inc.1996-08-23
K955356ACTIVE ULTRA-SENSITIVE UNCONJUGATED ESTRIOLDiagnostic Systems Laboratories, Inc.1996-05-15
K944490AUTODELFIA UNCONJUGATED ESTRIOL (UE3) KITWallac OY1994-12-09
K920576AMERLEX-M HIGH SENSITIVITY UNCONJUGATED ESTRIOLEastman Kodak Company1992-03-23
K903359MICROZYME UNCONJUGATED ESTRIOL ENZYME IMMUNO KITImmunotech Corp.1990-08-22
K860900IMMPULSE FREE ESTRIOL ASSAY REAGENTSSclavo, Inc.1986-04-28
K850787SOLID PHASE FREE ESTRIOL ENZYME IMMUNOASSAYNms Pharmaceuticals, Inc.1985-03-26
K844767RADIOIMMUNOASSAY OF HUMAN SERUM PLASMA OR URINE TOBiotecx Laboratories, Inc.1985-02-01
K844511TDX TOTAL ESTRIOLAbbott Laboratories1985-01-18
K844408AMERLEX-M SPECIFIC ESTRIOL UNCONJUGATEDAmersham Corp.1984-12-11
K840902ENDAB ESTRIOL UNCONJUGATEDImmunotech Corp.1984-04-18
K840301RIANEN ESTRIOL RADIOIMMUNOASSAY KITNew England Nuclear1984-03-30
K830816DSL 1900Diagnostic Systems1983-04-12
K823202FREE & TOTAL ESTRIOL KITDiagnostic Products Corp.1982-12-15