MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG — Medipurpose Pte. , Ltd. (510(k) K110062)
MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG — Medipurpose Pte. , Ltd. (510(k) K110062) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG; Applicant: Medipurpose Pte. , Ltd.; Clearance track: 510(
| Device name | MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG |
|---|---|
| Applicant | Medipurpose Pte. , Ltd. |
| Clearance track | 510(k) |
| Submission number | K110062 |
| Decision | Substantially Equivalent |
| Decision date | 2011-09-01 |
| Date received | 2011-01-10 |
| Product code | FRO |
| Device class | U |
| Medical specialty | Unknown |
| Applicant location | GA, US |
| Source | openFDA device |
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