Endotherapeutics
FDA 510(k) & PMA Approved Devices — 7 products
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Total Devices7
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K870855 | UROSCAN | FAP | 1987-06-09 | View |
| 510(k) | K860192 | ENDOPORT 5MM SINGLE-USE TROCAR AND SLEEVE | HET | 1986-03-17 | View |
| 510(k) | K860102 | MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE | FHP | 1986-02-12 | View |
| 510(k) | K860103 | MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE | GCP | 1986-02-12 | View |
| 510(k) | K852031 | ENDOPORT 5MM | HET | 1985-08-13 | View |
| 510(k) | K844619 | ENDONEEDLE | FHO | 1985-01-09 | View |
| 510(k) | K841716 | ENDOPORT EROCAR | FBQ | 1984-06-28 | View |
No matching devices.
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