I-Stat System

FDA 510(k) K011478 · I-Stat Corp.

Substantially Equivalent

510(k) numberK011478

Submission

Device name
I-Stat System
Applicant
I-Stat Corp.
East Windsor, NJ, US
Received
May 14, 2001
Decision date
July 2, 2001
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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K093297Epoc Bgem, Epoc Reader, Epoc Host, Epoc Care-Fill Capillary TubeKHP · Traditional Epocal, Inc.06/09/2010SE
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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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K053597I-Stat B-Type Natriuretic Peptide (BNP)NBC · Traditional 07/21/2006SE
K053110Abbott i-STAT Crea Cartridge, Abbott i-STAT G Cartridge, Abbott i-STAT 6+ Cartridge…JGS · Special 01/13/2006SE
K051433I-Stat Creatine Kinase MB (Ck-Mb)MYT · Traditional 12/15/2005SE
K031873I-Stat Cardiac Markers Control Level 1, 2, and 3; Cardiac Markers Calibration…JJX · Traditional 10/07/2003SE
K023582I-Stat Kaolin Act TestJBP · Traditional 09/08/2003SE
K031739I-Stat Cardiac Troponin (Ctni) TestMMI · Traditional 09/02/2003SE
K020355I-Stat Prothrombin Time TestGJS · Traditional 05/14/2002SE
K012478Modification to: I-Stat Portable Clinical AnalyzerCHL · Special 08/20/2001SE
K001387I-Stat Portable Clinical Analyzer, Model 300CGA · Traditional 10/05/2000SE
K001154I-Stat Model 200 Portable Clinical AnalyzerJGS · Special 04/18/2000SE

Questions and answers

When was I-Stat System cleared by the FDA?

I-Stat System (K011478) received a 510(k) decision of Substantially Equivalent on July 2, 2001, 49 days after the submission was received.

What is the product code of K011478?

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