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 Mansfield Scientific with 8 510(k) clearances. The most recent is a 510(k) clearance dated Dec 15, 1987: ANGIOSCOPE.
| Dec 15, 1987 | ANGIOSCOPEK865017 · DQX | 510(k) clearances |
| Feb 20, 1987 | ENDOMYOCARDIAL BIOPSY DEVICEK870186 · DWZ | 510(k) clearances |
| Feb 18, 1986 | CIRIBART GYUDUBG CATGETERK855103 · DQO | 510(k) clearances |
| Dec 4, 1985 | EXPLORERK853850 · DTB | 510(k) clearances |
| Sep 16, 1985 | HEPARIN COAT TRAN BALLO TIP TEMP PAC ELECTRODEK852797 · LDF | 510(k) clearances |
| Jul 19, 1985 | PERCUTANEOUS TRANSLUMINAL BLOOD DILATION CATHETERK851848 · LIT | 510(k) clearances |
| Jan 2, 1985 | TRANSVENOUS BALLOON TIPPED(FLOW DIRECTED) TEMP. PAK844752 · DTB | 510(k) clearances |
| Jul 13, 1984 | WEDGE PRESSURE CATHETER FLOW DIRECTEDK841705 · DYG | 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
