FDA 510(k) Applications Submitted by ASTORIA-PACIFIC,INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090940 |
04/03/2009 |
SPOTCHECK BLOOD SPOT CONTROL, ASSAYED |
ASTORIA-PACIFIC,INC. |
| K121101 |
04/11/2012 |
SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT |
ASTORIA-PACIFIC,INC. |
| K080294 |
02/04/2008 |
ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KIT |
ASTORIA-PACIFIC,INC. |
| K101392 |
05/18/2010 |
NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350D |
ASTORIA-PACIFIC,INC. |
| K102643 |
09/14/2010 |
SPOTCHECK NEONATAL GALT MICROPLATE REAGENT KIT |
ASTORIA-PACIFIC,INC. |
| K970093 |
01/10/1997 |
TYROSINE 50-HOUR REAGENT KIT |
ASTORIA-PACIFIC,INC. |
| K970277 |
01/23/1997 |
URIDYLTRANSFERASE KIT, 50 HOUR (80-4000-13K) |
ASTORIA-PACIFIC,INC. |
| K010844 |
03/21/2001 |
ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE KIT, 50 HOUR, PART NO. 80-8000-13K |
ASTORIA-PACIFIC,INC. |
| K990957 |
03/22/1999 |
ASTORIA-PACIFIC SPOTCHECK G6PD KIT 50 HR, MODEL 80-3000-13K |
ASTORIA-PACIFIC,INC. |
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