Piccolo Lactate Test System

FDA 510(k) K130113 · Abaxis, Inc.

Substantially Equivalent

510(k) numberK130113

Submission

Device name
Piccolo Lactate Test System
Applicant
Abaxis, Inc.
Union City, CA, US
Received
January 16, 2013
Decision date
March 11, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KHP – Acid, Lactic, Enzymatic Method
Device class
Class I (low risk)
Regulation
21 CFR 862.1450
Specialty
Clinical Chemistry

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K112430I-Stat Lactate Test/I-Sat CG4+CARTRIDGEKHP · Traditional Abbott Pont of Care, Inc.12/20/2011SE
K100602Nova Statstrip Lactate Hospital Meter, Nova Statstrip Lactate Test StripsKHP · Traditional Nova Biomedical Corp.08/17/2011SE
K093297Epoc Bgem, Epoc Reader, Epoc Host, Epoc Care-Fill Capillary TubeKHP · Traditional Epocal, Inc.06/09/2010SE
K013938Irma SL Blood Analysis System Lactate CartridgeKHP · Traditional Diametrics Medical, Inc.01/28/2002SE
K011478I-Stat SystemKHP · Traditional I-Stat Corp.07/02/2001SE
K980908Lactate Pro SystemKHP · Traditional Kdk Corp.09/11/1998SE
K982071I-Stat Lactate TestKHP · Traditional I-Stat Corp.06/29/1998SE
K971944Lactest IKHP · Traditional Jwt, Inc.12/17/1997SE

More from Jwt, Inc.

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K120664Piccolo Trglycerides-Capillary Test SystemJGY · Traditional 04/24/2012SE
K120662Piccolo Hdl-Capillary Test SystemJHM · Traditional 04/24/2012SE
K091052Piccolo C-Reactive Protein (CRP) Test SystemDCN · Traditional 01/15/2010SE
K091910Piccolo Magnesium Test SystemJGJ · Special 10/01/2009SE
K051108Piccolo Lactate Dephydrogenase Test SystemCFJ · Traditional 07/08/2005SE
K040115Piccolo Magnesium Test SystemJGJ · Traditional 01/30/2004SE
K023642Piccolo Total Cholesterol Test SystemCHH · Traditional 01/24/2003SE
K023640Piccolo HDL Test SystemLBS · Traditional 01/24/2003SE

Questions and answers

When was Piccolo Lactate Test System cleared by the FDA?

Piccolo Lactate Test System (K130113) received a 510(k) decision of Substantially Equivalent on March 11, 2013, 54 days after the submission was received.

What is the product code of K130113?

The FDA product code is KHP – Acid, Lactic, Enzymatic Method, a Class I (low risk) device regulated under 21 CFR 862.1450.