Astoria-Pacific, Inc. is one of 5196 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Astoria-Pacific, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Astoria-Pacific, Inc. has 9 FDA 510(k) cleared medical devices. Based in Clakamas, US.
Historical record: 9 cleared submissions from 1997 to 2013. Primary specialty: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Astoria-Pacific, Inc. Filter by specialty or product code using the sidebar.
Astoria-Pacific, Inc. — FDA 510(k) Products and Clearance History
9 devices
Cleared
Jun 20, 2013
SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT
Chemistry
435d
Cleared
Jul 15, 2011
SPOTCHECK NEONATAL GALT MICROPLATE REAGENT KIT
Chemistry
304d
Cleared
Feb 04, 2011
NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350D
Chemistry
262d
Cleared
Dec 14, 2009
SPOTCHECK BLOOD SPOT CONTROL, ASSAYED
Chemistry
255d
Cleared
Nov 04, 2008
ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KIT
Chemistry
274d
Cleared
Sep 21, 2001
ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE KIT, 50 HOUR, PART NO. 80-8000-13K
Chemistry
184d
Cleared
May 11, 1999
ASTORIA-PACIFIC SPOTCHECK G6PD KIT 50 HR, MODEL 80-3000-13K
Hematology
50d
Cleared
Mar 19, 1998
TYROSINE 50-HOUR REAGENT KIT
Chemistry
433d
Cleared
Dec 11, 1997
URIDYLTRANSFERASE KIT, 50 HOUR (80-4000-13K)
Chemistry
322d