Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in FinlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of General ElectricLabelled 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 Instrumentarium with 20 510(k) clearances. The most recent is a 510(k) clearance dated Oct 9, 2002: MODIFICATION TO FOCUS.
| Oct 9, 2002 | MODIFICATION TO FOCUSK022630 · EHD | 510(k) clearances |
| Jul 13, 2000 | FOCUSK001729 · EHD | 510(k) clearances |
| Jun 22, 2000 | ORTHOCEPH OC100 DK001439 · MUH | 510(k) clearances |
| Sep 28, 1999 | ORTHOPANTOMOGRAPH OP100DK992385 · MUH | 510(k) clearances |
| Jul 17, 1998 | MAMMOGRAPHY X-RAY EQUIPMENT MODELS MGF101 AND MGF110, ALPHA III, ALPHA ST, ALPHA RT AND ALPHA IQK981641 · IZH | 510(k) clearances |
| Apr 4, 1997 | TONOCAP, TC-200 AND ACCESSORY CATHETERSK962638 · CCK | 510(k) clearances |
| Apr 30, 1996 | TONOMETERED SLAINE BLOOD GAS CONTROLK961441 · JJS | 510(k) clearances |
| Jan 30, 1996 | TRIP NGS & SIGMOID CATHETER PHI SLIDE CALCULATORK955018 · FFT | 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
