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 15, 2026, FDA's public records list Brentwood Instruments with 21 510(k) clearances. The most recent is a 510(k) clearance dated Mar 1, 1990: SPIROSCAN 4000.
| Mar 1, 1990 | SPIROSCAN 4000K896924 · BZG | 510(k) clearances |
| Aug 2, 1988 | RHYTHMSCAN HR HOLTER RECORDERK882366 · DSH | 510(k) clearances |
| Feb 22, 1988 | RHYTHMSCANK871572 · DSI | 510(k) clearances |
| Mar 31, 1986 | FUKUDA DENSHI CARDIMAX FCP-211K860024 · DSI | 510(k) clearances |
| Feb 6, 1986 | CARDIMAX FX-1164K853979 · DPS | 510(k) clearances |
| Feb 4, 1986 | CARDIMAX FX-406UK854505 · DRS | 510(k) clearances |
| Jul 1, 1985 | SPIRO SCANK851135 · BZG | 510(k) clearances |
| May 15, 1985 | T-1000 ECG TRANSMITTERK851124 · DXH | 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
