MODIFICATION TO: HI-ART SYSTEM — Tomotherapy Incorporated (510(k) K033347)
MODIFICATION TO: HI-ART SYSTEM — Tomotherapy Incorporated (510(k) K033347) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: MODIFICATION TO: HI-ART SYSTEM; Applicant: Tomotherapy Incorporated; Clearance track: 510(k).
| Device name | MODIFICATION TO: HI-ART SYSTEM |
|---|---|
| Applicant | Tomotherapy Incorporated |
| Clearance track | 510(k) |
| Submission number | K033347 |
| Decision | Substantially Equivalent |
| Decision date | 2003-11-12 |
| Date received | 2003-10-20 |
| Product code | IYE |
| Device class | 2 |
| Medical specialty | Radiology |
| Applicant location | WI, US |
| Source | openFDA device |
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$1999/mo
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