Diagnostics makerLabelled 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 13, 2026, FDA's public records list Aesku, Inc. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Dec 13, 2006: AESKULSKA BETA2-GLYCO-A.
| Date | Record | Source |
|---|---|---|
| Dec 13, 2006 | AESKULSKA BETA2-GLYCO-AK062217 · MSV | 510(k) clearances |
| Nov 14, 2005 | AESKULISA ASCA AK051492 · NBT | 510(k) clearances |
| Jun 1, 2005 | AESKULISA TTG A AND AESKULISA TTG GK042644 · MVM | 510(k) clearances |
| Jun 23, 2004 | AESKULISA ANA HEP-2K040953 · LJM | 510(k) clearances |
| May 12, 2004 | AESKULISA CARDIOLIPIN AGMK040463 · MID | 510(k) clearances |
| Dec 16, 2003 | AESKULISA ANA 8PROK032469 · LLL | 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
