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

PICCOLO MAGNESIUM TEST SYSTEM

K Number: K091910 · Decision Oct 1, 2009
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
20
Review Days
98

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Basic Information

Device Name
PICCOLO MAGNESIUM TEST SYSTEM
K Number
K091910
Device Class
FDA class 1
Clearance Type
Special
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Abaxis, Inc.
Date Received
June 25, 2009
Decision Date
October 1, 2009
Product Code
JGJ
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
JGJ Photometric Method, Magnesium

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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
K051108 PICCOLO LACTATE DEPHYDROGENASE TEST SYSTEM
K040115 PICCOLO MAGNESIUM TEST SYSTEM
K023640 PICCOLO HDL TEST SYSTEM
K023642 PICCOLO TOTAL CHOLESTEROL TEST SYSTEM
Search all 20 clearances from Abaxis, Inc. →