DIOSCAN — Diomed, Inc. (510(k) K990014)
DIOSCAN — Diomed, Inc. (510(k) K990014) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: DIOSCAN; Applicant: Diomed, Inc.; Clearance track: 510(k).
| Device name | DIOSCAN |
|---|---|
| Applicant | Diomed, Inc. |
| Clearance track | 510(k) |
| Submission number | K990014 |
| Decision | Substantially Equivalent |
| Decision date | 1999-02-26 |
| Date received | 1999-01-04 |
| Product code | GEX |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | MA, US |
| Source | openFDA device |
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$1999/mo
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