GSP Neonatalgalt Kit, Model 3303-001U

FDA 510(k) K100101 · Perkinelmer, Inc.

Substantially Equivalent

510(k) numberK100101

Submission

Device name
GSP Neonatalgalt Kit, Model 3303-001U
Applicant
Perkinelmer, Inc.
Indianapolis, IN, US
Received
January 13, 2010
Decision date
June 11, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KQP – Fluorescent Proc. (Qual.), Galactose-1-Phosphate Uridyl Transferase
Device class
Class II (moderate risk)
Regulation
21 CFR 862.1315
Specialty
Clinical Chemistry

Other 510(k)s with product code KQP

510(k)DeviceApplicantDecision
K102643Spotcheck Neonatal Galt Microplate Reagent KitKQP · Traditional Astoria-Pacific, Inc.07/15/2011SE
K101392Neopac Software, 3007 Digital Photometer/Fluorometer Model Na, 307 and 350DKQP · Traditional Astoria-Pacific, Inc.02/04/2011SE
K993536Bio-Rad Coda Neonatal Galt AssayKQP · Special Bio-Rad11/04/1999SE
K990827Microplate Neonatal Galt AssayKQP · Special Bio-Rad04/09/1999SE
K970277Uridyltransferase Kit, 50 Hour (80-4000-13K)KQP · Traditional Astoria-Pacific, Inc.12/11/1997SE
K894011Total GalactoseKQP · Traditional Alpkem Corp.01/11/1990SE

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Questions and answers

When was GSP Neonatalgalt Kit, Model 3303-001U cleared by the FDA?

GSP Neonatalgalt Kit, Model 3303-001U (K100101) received a 510(k) decision of Substantially Equivalent on June 11, 2010, 149 days after the submission was received.

What is the product code of K100101?

The FDA product code is KQP – Fluorescent Proc. (Qual.), Galactose-1-Phosphate Uridyl Transferase, a Class II (moderate risk) device regulated under 21 CFR 862.1315.