Loseff Medical Designers, Ltd.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K802025 | BALLOON RETENTION CHEST CATHETER | GBA | 1980-09-26 | View |
| 510(k) | K801349 | LOSEFF BALLOON TYPE SELF-RETENTION WOUND | JCX | 1980-08-07 | View |
No matching devices.
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