Lca, Inc.
FDA 510(k) & PMA Approved Devices — 12 products
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Total Devices12
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K952792 | PADLESS ELECTROSURGICAL PENCIL | GEI | 1995-08-28 | View |
| 510(k) | K944091 | THE HOOK-CURVED CLOSED END/ELECT FIBER LASER DELIV SYS | GEX | 1994-10-07 | View |
| 510(k) | K935439 | SNJ SMOKE EVACUATION SUCTION WAND | FYD | 1994-03-07 | View |
| 510(k) | K935258 | HYBRID SURGICAL DEVICE MODIFICATION | GEX | 1994-01-13 | View |
| 510(k) | K925726 | ALLOY SCALPEL HANDPIECES, MODIFICATION | GEX | 1993-11-22 | View |
| 510(k) | K931070 | CLOSED END FIBEROPTIC LASER DELIVERY SYSTEM | GEX | 1993-10-05 | View |
| 510(k) | K924160 | HYBRID SURGICAL DEVICE | GEX | 1993-04-23 | View |
| 510(k) | K923991 | ZOE LASER, CONTACT ND:YAG LASER SYSTEM | GEX | 1993-03-31 | View |
| 510(k) | K924120 | MOLDED FIBER CAP DELIVERY SYSTEM | GEX | 1993-03-19 | View |
| 510(k) | K901365 | LASER FORCEPS HANDPIECE | GEX | 1990-08-21 | View |
| 510(k) | K902562 | REVISED LABELING FOR MODEL CL-0PE ND:YAG LASER | GEX | 1990-06-20 | View |
| 510(k) | K900128 | CL-OPE CONTACT LASER SYSTEM | GEX | 1990-04-16 | View |
No matching devices.
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