Astoria-Pacific, Inc.
Astoria-Pacific, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2013.
Top product codes for Astoria-Pacific, Inc.
Recent clearances by Astoria-Pacific, Inc.
- K121101 — SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT
- K102643 — SPOTCHECK NEONATAL GALT MICROPLATE REAGENT KIT
- K101392 — NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350D
- K090940 — SPOTCHECK BLOOD SPOT CONTROL, ASSAYED
- K080294 — ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KIT
- K010844 — ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE KIT, 50 HOUR, PART NO. 80-8000-13K
- K990957 — ASTORIA-PACIFIC SPOTCHECK G6PD KIT 50 HR, MODEL 80-3000-13K
- K970093 — TYROSINE 50-HOUR REAGENT KIT
- K970277 — URIDYLTRANSFERASE KIT, 50 HOUR (80-4000-13K)
Data sourced from openFDA. This site is unofficial and independent of the FDA.