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

N-TACT PTH BY IMMUNORADIOMETRIC ASSAY (IRMA)

K Number: K874299 · Decision Nov 23, 1987
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
85
Applicant Total
58
Review Days
34

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Basic Information

Device Name
N-TACT PTH BY IMMUNORADIOMETRIC ASSAY (IRMA)
K Number
K874299
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1545
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Incstar Corp.
Date Received
October 20, 1987
Decision Date
November 23, 1987
Product Code
CEW
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
CEW Radioimmunoassay, Parathyroid Hormone

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K953567 INCSTAR 25-HYDROXYVITMIN D 1251 RIA
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K955363 INCSTAR HSZ I/II IGG ELISA ASSAY
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