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

HCG RIA TEST SYSTEM

K Number: K854958 · Decision Jan 28, 1986
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
21
Review Days
48

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Basic Information

Device Name
HCG RIA TEST SYSTEM
K Number
K854958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Monobind
Date Received
December 11, 1985
Decision Date
January 28, 1986
Product Code
JHI
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
JHI Visual, Pregnancy Hcg, Prescription Use

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Other Clearances by Monobind

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K980088 T-UPTAKE MICROPLATE EIA
K972720 FOLLICLE STIMULATING HORMONE (FSH) MICROPLATE ELISA (425-300)
K971834 ANTI-THYROID PEROXIDASE (TPO) MICROPLATE ELISA
K971835 ANTI-THYROGLOBULIN (TG) MICROPLATE ELISA
K971780 THYROTROPIN(TSH) ELISA
K971921 PROLACTIN (PRL) HORMONE MICROPLATE ELISA
K971779 TOTAL TRIIODOTHYRONINE(T3) MICROPLATE EIA
K971709 TOTAL THROXINE MICROPLATE EIA(225-300)
Search all 21 clearances from Monobind →