Medical device 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 Ashai Co., Ltd. with 12 510(k) clearances. The most recent is a 510(k) clearance dated May 15, 1987: AEROSOL ONE, NEBULIZER PUMP.
| Date | Record | Source |
|---|---|---|
| May 15, 1987 | AEROSOL ONE, NEBULIZER PUMPK870428 · BTI | 510(k) clearances |
| Apr 24, 1986 | AEROSOL ONEK852622 · BTI | 510(k) clearances |
| Oct 31, 1985 | SAFE.N.SUREK852620 · HIS | 510(k) clearances |
| Sep 26, 1985 | MAXI-NEBK852627 · CCQ | 510(k) clearances |
| Sep 18, 1985 | NASAL ONEK852628 · CAT | 510(k) clearances |
| Sep 18, 1985 | OXY-TWOK852624 · BYG | 510(k) clearances |
| Sep 18, 1985 | OXY-TUBEK852625 · CAT | 510(k) clearances |
| Sep 18, 1985 | AERO-MASK TWOK852629 · BYG | 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
