Lukens Corp.
FDA 510(k) & PMA Approved Devices — 11 products
Advertisement
Total Devices11
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K880230 | SIXALYZER | IKK | 1988-03-16 | View |
| 510(k) | K800102 | STANFORD STERILE LAP SPONGES | GDY | 1980-01-28 | View |
| 510(k) | K792471 | STANFORD STERILE LAP SPONGES | GDY | 1979-12-20 | View |
| 510(k) | K791495 | LUKENS BONE WAX (GAMMA RADIATION) | MTJ | 1979-09-24 | View |
| 510(k) | K770797 | TRAY, CATHETERIZATION W/FOLEY, STERILE | FRG | 1977-07-11 | View |
| 510(k) | K770795 | SHAVE PREP SET | JJX | 1977-07-11 | View |
| 510(k) | K770799 | TRAY, IRRIGATION, STERILE, BASIC | KKX | 1977-06-22 | View |
| 510(k) | K770796 | SKIN SCRUB PREP SET | KKX | 1977-06-22 | View |
| 510(k) | K770794 | SUTURE REMOVAL SET, STERILE | KDC | 1977-05-06 | View |
| 510(k) | K770800 | HANDLES, BLADE, SURGICAL | GES | 1977-05-06 | View |
| 510(k) | K770798 | BLADES, SURGICAL, STERILE | GES | 1977-05-06 | View |
No matching devices.
Advertisement