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Astoria-Pacific, Inc.

FDA 510(k) & PMA Approved Devices — 9 products

Total Devices9

Categories0

Latest FDA decision

Type	Number	Device Name	Code	Date	Actions
510(k)	K121101	SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT	JIA	2013-06-20	View
510(k)	K102643	SPOTCHECK NEONATAL GALT MICROPLATE REAGENT KIT	KQP	2011-07-15	View
510(k)	K101392	NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350D	KQP	2011-02-04	View
510(k)	K090940	SPOTCHECK BLOOD SPOT CONTROL, ASSAYED	JJT	2009-12-14	View
510(k)	K080294	ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KIT	NAK	2008-11-04	View
510(k)	K010844	ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE KIT, 50 HOUR, PART NO. 80-8000-13K	NAK	2001-09-21	View
510(k)	K990957	ASTORIA-PACIFIC SPOTCHECK G6PD KIT 50 HR, MODEL 80-3000-13K	JBL	1999-05-11	View
510(k)	K970093	TYROSINE 50-HOUR REAGENT KIT	CDR	1998-03-19	View
510(k)	K970277	URIDYLTRANSFERASE KIT, 50 HOUR (80-4000-13K)	KQP	1997-12-11	View

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