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

RADIOIMMUNOASSAY KIT(CORTISOL IN PLASMA)

K Number: K761346 · Decision Jan 7, 1977
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
83
Applicant Total
18
Review Days
10

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Basic Information

Device Name
RADIOIMMUNOASSAY KIT(CORTISOL IN PLASMA)
K Number
K761346
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1205
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
New England Nuclear
Date Received
December 28, 1976
Decision Date
January 7, 1977
Product Code
CGR
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
CGR Radioimmunoassay, Cortisol

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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
K781888 ASSAY SYSTEM, FERRITIN I KIT
Search all 18 clearances from New England Nuclear →