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

RIA, INSULIN, DOUBLE ANTIBODY

K Number: K790630 · Decision Jul 24, 1979
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
26
Applicant Total
9
Review Days
119

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Basic Information

Device Name
RIA, INSULIN, DOUBLE ANTIBODY
K Number
K790630
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1405
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Endocrine-Metabolic Center
Date Received
March 27, 1979
Decision Date
July 24, 1979
Product Code
CFP
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
CFP Radioimmunoassay, Immunoreactive Insulin

Similar 510(k) Clearances

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

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Other Clearances by Endocrine-Metabolic Center

K Number Device Name
K821131 RADIOIMMUNOASSAY PARATHYROID HORMONE MID
K811993 RADIOIMMUNOASSAY, FOLLICLE STIMULATING
K811994 RADIOIMMUNOASSAY LUTEINIZING HORMONE
K810948 RADIOIMMUNOASSAY THYROID STIM. HORM. KIT
K810351 RADIOIMMUNOASSAY, TOTAL TRIIODOTHRONIE
K800188 EMC-M-180, T3 UPTAKE - 100 TUBES
K800187 EMC-M-175, THYROXINE - 100 TUBES
K790602 RIA, DIGNXIN-125-I