Endolap, Inc.
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) | K974516 | ENDOLAP RESECTOSCOPE CUTTING LOOP ELECTRODE | FAS | 1997-12-22 | View |
| 510(k) | K974515 | ENDOLAP RESECTOSCOPE ROLLER ELECTRODE | FAS | 1997-12-22 | View |
| 510(k) | K950243 | TITAN INSUFFLATION NEEDLE | GCJ | 1995-04-06 | View |
| 510(k) | K950219 | ENDOLAP INSUFFLATOR TUBING SET | HIF | 1995-03-23 | View |
| 510(k) | K933492 | ESYS SYSTEM | HET | 1994-03-25 | View |
No matching devices.
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