Picore — Bio-Med USA, Inc. (510(k) K212082)
Picore — Bio-Med USA, Inc. (510(k) K212082) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: Picore; Applicant: Bio-Med USA, Inc.; Clearance track: 510(k).
| Device name | Picore |
|---|---|
| Applicant | Bio-Med USA, Inc. |
| Clearance track | 510(k) |
| Submission number | K212082 |
| Decision | Substantially Equivalent |
| Decision date | 2021-10-06 |
| Date received | 2021-07-02 |
| Product code | GEX |
| Device class | 2 |
| Medical specialty | General, Plastic Surgery |
| Applicant location | NJ, US |
| Source | openFDA device |
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