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

PICCOLO HDL TEST SYSTEM

K Number: K023640 · Decision Jan 24, 2003
Classifications
1
FEI Numbers
45
Registration Numbers
45
Same Product Code
79
Applicant Total
20
Review Days
86

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Basic Information

Device Name
PICCOLO HDL TEST SYSTEM
K Number
K023640
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1475
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Abaxis, Inc.
Date Received
October 30, 2002
Decision Date
January 24, 2003
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

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Other Clearances by Abaxis, Inc.

K Number Device Name
K200865 Piccolo Potassium Test System
K130113 PICCOLO LACTATE TEST SYSTEM
K130200 PICCOLO TOTAL CHOLESTEROL - CAPILLARY TEST SYSTEM
K120664 PICCOLO TRGLYCERIDES-CAPILLARY TEST SYSTEM
K120662 PICCOLO HDL-CAPILLARY TEST SYSTEM
K091052 PICCOLO C-REACTIVE PROTEIN (CRP) TEST SYSTEM
K091910 PICCOLO MAGNESIUM TEST SYSTEM
K051108 PICCOLO LACTATE DEPHYDROGENASE TEST SYSTEM
K040115 PICCOLO MAGNESIUM TEST SYSTEM
K023642 PICCOLO TOTAL CHOLESTEROL TEST SYSTEM
Search all 20 clearances from Abaxis, Inc. →