Atlas FDA

QUANTIMUNE HFSH RIA

FDA 510(k) clearance K791836 · decided 1979-10-01

Clearance details

K-number
K791836
Device name
QUANTIMUNE HFSH RIA
Applicant
Bio-Rad
Decision
Substantially Equivalent
Date received
1979-09-14
Decision date
1979-10-01
Days to decision
17 days
Clearance type
Traditional
Product code
CGJ
Device class
1
Regulation number
862.1300
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Mchenry, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
ONE STEP FSH MENOPAUSAL TEST (K052662)Ind Diagnostic, Inc.2005-11-30
MOMENTS MENOPAUSE CHECK, MODEL 9113 (K043599)Phamatech, Inc.2005-02-25
FSH MENOPAUSE PREDICTOR TEST (K041165)ACON Laboratories, Inc.2004-06-17
PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112 (K040575)Phamatech, Inc.2004-05-20
EARLYDETECT MENOPAUSE TEST FOR FSH (K030058)Early Detect, Inc.2003-07-30
GENUA MENOPAUSE MONITOR TEST KIT (K002450)Genua 1944, Inc.2001-01-12
FOLLICLE STIMULATING HORMONE (FSH) MICROPLATE ELISA (425-300) (K972720)Monobind1997-09-02
SEALITE SCIENCES AQUALITE FSH (K970085)Sealite Sciences, Inc.1997-02-14
VITROS IMMUNODIAGNOSTICS PRODUCTS FSH REAGENT PACK (GEM. 1005) FSH CALIBRATORS (GEM.C005) (K964720)Johnson & Johnson Clinical Diagnostics, Inc.1997-02-04
ELECSYS FSH ASSAY (K964693)Boehringer Mannheim Corp.1996-12-16
DSL ACTIVE FSH IRMA (K962118)Diagnostic Systems Laboratories, Inc.1996-09-09
AMERLITE FSH ASSAY (K952285)Johnson & Johnson Clinical Diagnostics, Inc.1995-07-03

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032/S002)Bio-Rad1996-03-01
BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032/S001)Bio-Rad1991-03-14
BIO-RAD CYCLOSPORINE BY HPLC TEST (P880032)Bio-Rad1989-07-24