Lactate Reagent

FDA 510(k) K840778 · American Dade

Substantially Equivalent

510(k) numberK840778

Submission

Device name
Lactate Reagent
Applicant
American Dade
Mchenry, IL, US
Received
February 8, 1984
Decision date
April 13, 1984
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K112955Nova Statstrip Lactate Hospital Meter SystemKHP · Traditional Nova Biomedical Corporation01/05/2012SE
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

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Questions and answers

When was Lactate Reagent cleared by the FDA?

Lactate Reagent (K840778) received a 510(k) decision of Substantially Equivalent on April 13, 1984, 65 days after the submission was received.

What is the product code of K840778?

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