Mas Tox Ammonia Controlliquid Assayed Tox Ammonia Control

FDA 510(k) K031392 · Medical Analysis Systems, Inc.

Substantially Equivalent

510(k) numberK031392

Submission

Device name
Mas Tox Ammonia Controlliquid Assayed Tox Ammonia Control
Applicant
Medical Analysis Systems, Inc.
Camarillo, CA, US
Received
May 2, 2003
Decision date
July 1, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DKC – Alcohol Control Materials
Device class
Class I (low risk)
Regulation
21 CFR 862.3280
Specialty
Clinical Toxicology

Other 510(k)s with product code DKC

510(k)DeviceApplicantDecision
K935819Quality Control Material (Assayed)DKC · Traditional Columbia Diagnostics, Inc.03/22/1994SE
K933425Ammonia/Ethanol Controls, High/Low, Cat.# A7937/7812DKC · Traditional Sigma Diagnostics, Inc.11/16/1993SE
K934467Beckman CX Ammonia/Alcohol ControlDKC · Traditional Beckman-Diagnostic Systems Group10/27/1993SE
K932067Ethanol Controls, Urine, Levels 1,II, and IIIDKC · Traditional Sigma Diagnostics, Inc.06/16/1993SE
K912827Serum Alcohol Control Levels 1, 2 & 3DKC · Traditional Cala Diagnostics08/12/1991SE
K912826Whole Blood Alcohol Control, Level 1 & 2DKC · Traditional Cala Diagnostics07/26/1991SE
K843872Ethanol Controls Low & High E5133/E5258DKC · Traditional Sigma Chemical Co.10/31/1984SE
K833514Toxi Chem Serum Alcohol ControlDKC · Traditional Fisher Diagnostics12/08/1983SE
K810465Emit-St Ethyl Alcohol Serum ControlsDKC · Traditional Syva Co.03/06/1981SE
K802618Emit-Stm Ethyl Alcohol Urine ControlsDKC · Traditional Syva Co.10/31/1980SE

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Questions and answers

When was Mas Tox Ammonia Controlliquid Assayed Tox Ammonia Control cleared by the FDA?

Mas Tox Ammonia Controlliquid Assayed Tox Ammonia Control (K031392) received a 510(k) decision of Substantially Equivalent on July 1, 2003, 60 days after the submission was received.

What is the product code of K031392?

The FDA product code is DKC – Alcohol Control Materials, a Class I (low risk) device regulated under 21 CFR 862.3280.