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

QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD

K Number: K890027 · Decision Apr 26, 1989
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
229
Applicant Total
12
Review Days
112

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Basic Information

Device Name
QUIKREAD CHEM. ANALYZER & CHOLES. FOR WHOLE BLOOD
K Number
K890027
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1175
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Photec Diagnostics, Inc.
Date Received
January 4, 1989
Decision Date
April 26, 1989
Product Code
CHH
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
CHH Enzymatic Esterase--Oxidase, Cholesterol

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
K892224 D-CHEM(TM) T-UPTAKE TEST KIT FOR T-UPTAKE DETERMIN
K890267 QUIKREAD CHEM. ANALYZER & CHOLES. FOR SERUM/PLASMA
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. →