FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ASSAY SYSTEM, FERRITIN I KIT

K Number: K781888 · Decision Jan 10, 1979
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
23
Applicant Total
18
Review Days
64

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
ASSAY SYSTEM, FERRITIN I KIT
K Number
K781888
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5340
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
New England Nuclear
Date Received
November 7, 1978
Decision Date
January 10, 1979
Product Code
JMG
Advisory Committee
Immunology
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
JMG Radioimmunoassay (Two-Site Solid Phase), Ferritin

Similar 510(k) Clearances

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

View all

Other Clearances by New England Nuclear

K Number Device Name
K841478 RIANEN CYCLIC-AMP RADIOIMMUNOASSAY
K840301 RIANEN ESTRIOL RADIOIMMUNOASSAY KIT
K834038 RIANEN FOLLICLE STIMULATING HORMONE
K833376 RIANEN LUTEINIZING HORMONE RIA KIT
K831345 RIANEN PROLACTIN 125I KIT
K801245 ATOMLIGHT (LIQUID SCINTILLATION SOLUTION
K792175 RIANEN, VITAMIN B12 ASSAY SYSTEM
K790817 RIA KIT, QUANTITATION OF PROSTATIC ACID
K782110 RIA KIT, RIANEN CORTISOL
K781495 RIANEN ASSAY SYSTEM, 125I KIT
Search all 18 clearances from New England Nuclear →