Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Astoria-Pacific with 9 510(k) clearances. The most recent is a 510(k) clearance dated Jun 20, 2013: SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KIT.
| Jun 20, 2013 | SPOTCHECK NEONATAL TOTAL GALACTOSE MICROPLATE REAGENT KITK121101 · JIA | 510(k) clearances |
| Jul 15, 2011 | SPOTCHECK NEONATAL GALT MICROPLATE REAGENT KITK102643 · KQP | 510(k) clearances |
| Feb 4, 2011 | NEOPAC SOFTWARE, 3007 DIGITAL PHOTOMETER/FLUOROMETER MODEL NA, 307 AND 350DK101392 · KQP | 510(k) clearances |
| Dec 14, 2009 | SPOTCHECK BLOOD SPOT CONTROL, ASSAYEDK090940 · JJT | 510(k) clearances |
| Nov 4, 2008 | ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE MICROPLATE REAGENT KITK080294 · NAK | 510(k) clearances |
| Sep 21, 2001 | ASTORIA-PACIFIC SPOTCHECK BIOTINIDASE KIT, 50 HOUR, PART NO. 80-8000-13KK010844 · NAK | 510(k) clearances |
| May 11, 1999 | ASTORIA-PACIFIC SPOTCHECK G6PD KIT 50 HR, MODEL 80-3000-13KK990957 · JBL | 510(k) clearances |
| Mar 19, 1998 | TYROSINE 50-HOUR REAGENT KITK970093 · CDR | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
