Ria System for Human F-S Hormone

FDA 510(k) K780870 · Calbiochem-Behring Corp.

Substantially Equivalent

510(k) numberK780870

Submission

Device name
Ria System for Human F-S Hormone
Applicant
Calbiochem-Behring Corp.
Mchenry, IL, US
Received
May 30, 1978
Decision date
June 22, 1978
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CGJ – Radioimmunoassay, Follicle-Stimulating Hormone
Device class
Class I (low risk)
Regulation
21 CFR 862.1300
Specialty
Clinical Chemistry

Other 510(k)s with product code CGJ

510(k)DeviceApplicantDecision
K052662One Step FSH Menopausal TestCGJ · Traditional Ind Diagnostic, Inc.11/30/2005SE
K043599Moments Menopause Check, Model 9113CGJ · Special Phamatech, Inc.02/25/2005SE
K041165FSH Menopause Predictor TestCGJ · Traditional ACON Laboratories, Inc.06/17/2004SE
K040575Pharmatech Menopause Check, Models 9111 and 9112CGJ · Traditional Phamatech, Inc.05/20/2004SE
K030058Earlydetect Menopause Test for FSHCGJ · Traditional Early Detect, Inc.07/30/2003SE
K002450Genua Menopause Monitor Test KitCGJ · Traditional Genua 1944, Inc.01/12/2001SE
K972720Follicle Stimulating Hormone (FSH) Microplate Elisa (425-300)CGJ · Traditional Monobind09/02/1997SE
K970085Sealite Sciences Aqualite FSHCGJ · Traditional Sealite Sciences, Inc.02/14/1997SE
K964720Vitros Immunodiagnostics Products FSH Reagent Pack (Gem. 1005) FSH Calibrators (GEM.C005)CGJ · Traditional Johnson & Johnson Clinical Diagnostics, Inc.02/04/1997SE
K964693Elecsys FSH AssayCGJ · Traditional Boehringer Mannheim Corp.12/16/1996SE

More from Boehringer Mannheim Corp.

510(k)DeviceDecision
K831811Revolution Radial Immunodiffusion PlateJZQ · Traditional 07/28/1983SE
K831036Ena Test Kit SM & RNP Auto AntibodyLLL · Traditional 04/27/1983SE
K830214Aft System IIIDHN · Traditional 03/09/1983SE
K820812Creatine Kinase-Mb KitJHY · Traditional 04/12/1982SE
K813493Enzygnost TM Rubella IgmLFX · Traditional 03/04/1982SE
K820088Aft System Proficiency Testing ProgramDBL · Traditional 01/26/1982SE
K812458PadacJTO · Traditional 09/23/1981SE
K810718C-Peptice ReagentsJKD · Traditional 03/31/1981SE
K810669Pantrak E.K.CIW · Traditional 03/31/1981SE
K810404Rheumatoid Factors Reference SerumDHR · Traditional 03/11/1981SE

Questions and answers

When was Ria System for Human F-S Hormone cleared by the FDA?

Ria System for Human F-S Hormone (K780870) received a 510(k) decision of Substantially Equivalent on June 22, 1978, 23 days after the submission was received.

What is the product code of K780870?

The FDA product code is CGJ – Radioimmunoassay, Follicle-Stimulating Hormone, a Class I (low risk) device regulated under 21 CFR 862.1300.