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

FOLLICLE STIMULATING HORMONE KIT

K Number: K820358 · Decision Mar 26, 1982
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
87
Applicant Total
29
Review Days
45

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
FOLLICLE STIMULATING HORMONE KIT
K Number
K820358
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Pcl-Ria, Inc.
Date Received
February 9, 1982
Decision Date
March 26, 1982
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 Pcl-Ria, Inc.

K Number Device Name
K830526 B-GCG SYSTEM BY RIA
K822935 THYROID STIMULATING HORMONE
K823014 DIGOXIN KIT
K822612 T3 UPTAKE KITS
K820886 THYROXINE T4 KIT
K820357 LUTEINIZING HORMONE KIT
K812666 THYROXINE (T4) 125I
K810867 FOLLICLE STIMULATING HORMONE (FSH)
K810852 FOLLICLE STIMULATING HORMONE ANTISERUM
K810754 LUTENIZING HORMONES
Search all 29 clearances from Pcl-Ria, Inc. →