Gynecare, A Div. of Ethicon, Inc.
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) | K040302 | VERSAPOINT RESECTOSCOPIC SYSTEM | HIH | 2004-03-09 | View |
| 510(k) | K013718 | GYNEMESH PROLENE SOFT (POLYPROPYLENE) NONABSORBABLE SYNTHETIC SURGICAL MESH FOR PELVIC FLOOR REPAIR | OTO | 2002-01-08 | View |
No matching devices.
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