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

RIANEN ESTRIOL RADIOIMMUNOASSAY KIT

K Number: K840301 · Decision Mar 30, 1984
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
41
Applicant Total
18
Review Days
66

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Basic Information

Device Name
RIANEN ESTRIOL RADIOIMMUNOASSAY KIT
K Number
K840301
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1265
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
New England Nuclear
Date Received
January 24, 1984
Decision Date
March 30, 1984
Product Code
CGI
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
CGI Radioimmunoassay, Estriol

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Other Clearances by New England Nuclear

K Number Device Name
K841478 RIANEN CYCLIC-AMP RADIOIMMUNOASSAY
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
K781495 RIANEN ASSAY SYSTEM, 125I KIT
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