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

D-CHEM(TM) T-UPTAKE TEST KIT FOR T-UPTAKE DETERMIN

K Number: K892224 · Decision Jun 16, 1989
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
92
Applicant Total
12
Review Days
74

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Basic Information

Device Name
D-CHEM(TM) T-UPTAKE TEST KIT FOR T-UPTAKE DETERMIN
K Number
K892224
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1715
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Photec Diagnostics, Inc.
Date Received
April 3, 1989
Decision Date
June 16, 1989
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

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Other Clearances by Photec Diagnostics, Inc.

K Number Device Name
K897169 QUIKREAD(R) WHOLE BLOOD TRIGLYCERIDE TEST KIT
K896329 D-CHEM TOTAL T4 TEST KIT FOR THYROXINE QUANTITA.
K894057 QUIKREAD WHOLE BLOOD HDL-CHOLESTEROL TEST KIT
K890267 QUIKREAD CHEM. ANALYZER & CHOLES. FOR SERUM/PLASMA
K890027 QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD
K882307 D-CHEM
K880291 THEOPHYLLINE TEST KIT REF. #A874799
K854875 APO-SCREEN CALIBRATOR & CONTROL SET FOR HDL APO A1
K853048 APO-SCREEN TEST SET FOR HDL-APOLIPOPTEIN A-1
K853174 APO-CHROME IMMUNOASSAY TEST SET FOR APOLIPOPROTEIN
Search all 12 clearances from Photec Diagnostics, Inc. →