Medipurpose Pte. , Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K222224 | SurgiLance® Safety Lancet | FMK | 2022-09-22 | View |
| 510(k) | K130132 | BABYLANCE HEEL INCISION DEVICE | FMK | 2013-02-11 | View |
| 510(k) | K110062 | MEDIPLUS-FOAM AG; MEDIPLUS-COMFORTFOAM AG; MEDIPLUS-SUPERFOAM AG | FRO | 2011-09-01 | View |
| 510(k) | K101145 | SURGILANCE SAFETY LANCETS, MODELS SLN100, SLN200, SLN240, SLN300, SLB200, SLB250 | FMK | 2010-10-21 | View |
| 510(k) | K101417 | BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200 | FMK | 2010-10-19 | View |
No matching devices.
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