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

T-UPTAKE MICROPLATE EIA

K Number: K980088 · Decision Feb 4, 1998
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
92
Applicant Total
21
Review Days
26

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Basic Information

Device Name
T-UPTAKE MICROPLATE EIA
K Number
K980088
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1715
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Monobind
Date Received
January 9, 1998
Decision Date
February 4, 1998
Product Code
KHQ
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
KHQ Radioassay, Triiodothyronine Uptake

Similar 510(k) Clearances

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

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Other Clearances by Monobind

K Number Device Name
K030860 ACCUBIND NEONATAL T4 MICROPLATE EIA, MODEL 2625-300
K020548 FREE T4 (THYTOXINE) MICROPLATE EIA TEST MODELS # 1225-300
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)
K926345 TRIODOTHYRONINE (TC) COATED TUBE RIA
Search all 21 clearances from Monobind →