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

QUIKREAD WHOLE BLOOD HDL-CHOLESTEROL TEST KIT

K Number: K894057 · Decision Aug 31, 1989
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
12
Review Days
85

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
QUIKREAD WHOLE BLOOD HDL-CHOLESTEROL TEST KIT
K Number
K894057
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Photec Diagnostics, Inc.
Date Received
June 7, 1989
Decision Date
August 31, 1989
Product Code
LBS
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
LBS Ldl & Vldl Precipitation, Cholesterol Via Esterase-Oxidase, Hdl

Similar 510(k) Clearances

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

View all

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.
K892224 D-CHEM(TM) T-UPTAKE TEST KIT FOR T-UPTAKE DETERMIN
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. →