510(k) K030058

Device
EARLYDETECT MENOPAUSE TEST FOR FSH
Applicant
Early Detect, Inc.
510(k) number
K030058
Product code
CGJ
Decision
Substantially Equivalent (SESE)
Decision date
2003-07-30
Date received
2003-01-07
Regulation
862.1300
Classification name
Radioimmunoassay, Follicle-Stimulating Hormone
Medical specialty
Clinical Chemistry
Review panel
Clinical Chemistry
Device class
1
Clearance type
Traditional
Statement or summary
Statement
Third party reviewed
N

Applicant Contact#

Contact
PETER GEORGE
Address
2950 N. Glassell St. Orange CA US 92865 92865

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code CGJ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K052662ONE STEP FSH MENOPAUSAL TESTInd Diagnostic, Inc.2005-11-30
K043599MOMENTS MENOPAUSE CHECK, MODEL 9113Phamatech, Inc.2005-02-25
K041165FSH MENOPAUSE PREDICTOR TESTACON Laboratories, Inc.2004-06-17
K040575PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112Phamatech, Inc.2004-05-20
K002450GENUA MENOPAUSE MONITOR TEST KITGenua 1944, Inc.2001-01-12
K972720FOLLICLE STIMULATING HORMONE (FSH) MICROPLATE ELISA (425-300)Monobind1997-09-02
K970085SEALITE SCIENCES AQUALITE FSHSealite Sciences, Inc.1997-02-14
K964720VITROS IMMUNODIAGNOSTICS PRODUCTS FSH REAGENT PACK (GEM. 1005) FSH CALIBRATORS (GEM.C005)Johnson & Johnson Clinical Diagnostics, Inc.1997-02-04
K964693ELECSYS FSH ASSAYBoehringer Mannheim Corp.1996-12-16
K962118DSL ACTIVE FSH IRMADiagnostic Systems Laboratories, Inc.1996-09-09
K952285AMERLITE FSH ASSAYJohnson & Johnson Clinical Diagnostics, Inc.1995-07-03
K943437AQUALITE FSHSealite Sciences, Inc.1994-12-28
K941221DUPONT ACA PLUS IMMUNOASSAY SYSTEM FOLLICLE STIMULATING HORMONEDupont Medical Products1994-07-20
K935612AXSYM FOLLICLE STIMULATING HORMONE (FSH)Abbott Laboratories1994-06-21
K940005ACCESS HUMAN FOLLICLE STIMULATING HORMONE ASSAYBio-Rad Laboratories, Inc.1994-03-03