TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560 — Somatex Medical Technologies GmbH (510(k) K073095)
TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560 — Somatex Medical Technologies GmbH (510(k) K073095) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560; Applicant: Somatex Medical Tech
| Device name | TUMARK PROFESSIONAL, MODEL 271560; MR- TUMARK PROFESSIONAL, MODEL 601560 |
|---|---|
| Applicant | Somatex Medical Technologies GmbH |
| Clearance track | 510(k) |
| Submission number | K073095 |
| Decision | Substantially Equivalent |
| Decision date | 2008-03-19 |
| Date received | 2007-11-01 |
| Product code | NEU |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | MA, US |
| Source | openFDA device |
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