Delfia Neonatal Irt Kit, Model A005-110

FDA 510(k) K003664 · Wallac OY

Substantially Equivalent

510(k) numberK003664

Submission

Device name
Delfia Neonatal Irt Kit, Model A005-110
Applicant
Wallac OY
Turku, FI
Received
November 28, 2000
Decision date
February 14, 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
CGZ – Electrode, Ion-Specific, Chloride
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1170
Specialty
Clinical Chemistry

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More from Phoenix Diagnostics, Inc.

510(k)DeviceDecision
K131284GSP Neonatal Biotinidase KitNAK · Traditional 11/14/2013SE
K100682GSP Neonatal 17A-OH-PROGESTERONE Kit Model: 3305-001UJLX · Traditional 07/23/2010SE
K081922Autodelfia Neonatal 17A-OH-PROGESTERONE KitJLX · Traditional 04/16/2009SE
K071649Neonatal Total Galactose Kit; Neontal Total Galactose Kit, Models 3029-0010 and 3029-110BJIA · Traditional 08/07/2008SE
K070889Autodelfia Neonatal Irt L Kit, Model B022-112CGZ · Traditional 04/14/2008SE
K050709Resolve Hemoglobin Kit, JB-2 Staining System, Models FR-9120, FR-9400, FR-9360, FR-9367GKA · Traditional 03/08/2006SE
K050960Modification to: Autodelfia Neonatal 17A-OH-PROGESTERONE L KitJLX · Special 07/11/2005SE
K042425Autodelfia Neonatal 17A-OH-PROGESTERONE KitJLX · Special 09/30/2004SE
K042424Delfia Neonatal 17A-OH-PROGESTERONE KitJLX · Special 09/30/2004SE
K003668Autodelfia Neonatal Irt Kit, Model B005-112CGZ · Traditional 02/12/2001SE

Questions and answers

When was Delfia Neonatal Irt Kit, Model A005-110 cleared by the FDA?

Delfia Neonatal Irt Kit, Model A005-110 (K003664) received a 510(k) decision of Substantially Equivalent on February 14, 2001, 78 days after the submission was received.

What is the product code of K003664?

The FDA product code is CGZ – Electrode, Ion-Specific, Chloride, a Class II (moderate risk) device regulated under 21 CFR 862.1170.