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 Biotrine Corp. with 6 510(k) clearances. The most recent is a 510(k) clearance dated Sep 11, 1992: ASTECH HOME PEAK FLOW METER.
| Date | Record | Source |
|---|---|---|
| Sep 11, 1992 | ASTECH HOME PEAK FLOW METERK915060 · BZH | 510(k) clearances |
| Nov 28, 1988 | MULTIICHALLENGE NEBULIZER SYSTEMK883704 · BTI | 510(k) clearances |
| Dec 15, 1986 | MULTISPIRO SA/100K863134 · BZG | 510(k) clearances |
| Nov 20, 1984 | B-1000K844226 · BZG | 510(k) clearances |
| Dec 31, 1981 | PEAK FLOW MONITORK813414 · BZH | 510(k) clearances |
| Oct 26, 1981 | FLO-COR IK812825 · JAX | 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
