FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

RIA SYSTEM FOR HUMAN F-S HORMONE

K Number: K780870 · Decision Jun 22, 1978
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
41
Review Days
23

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
RIA SYSTEM FOR HUMAN F-S HORMONE
K Number
K780870
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Calbiochem-Behring Corp.
Date Received
May 30, 1978
Decision Date
June 22, 1978
Product Code
CGJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CGJ Radioimmunoassay, Follicle-Stimulating Hormone

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CGJ), ordered by most recent decision date.

View all

Other Clearances by Calbiochem-Behring Corp.

K Number Device Name
K831811 REVOLUTION RADIAL IMMUNODIFFUSION PLATE
K831036 ENA TEST KIT SM & RNP AUTO ANTIBODY
K830214 AFT SYSTEM III
K820812 CREATINE KINASE-MB KIT
K813493 ENZYGNOST TM RUBELLA IGM
K820088 AFT SYSTEM PROFICIENCY TESTING PROGRAM
K812458 PADAC
K810718 C-PEPTICE REAGENTS
K810669 PANTRAK E.K.
K810309 RUBELLA ANTIBODIES TEST REAGENTS
Search all 41 clearances from Calbiochem-Behring Corp. →