Innovative Health
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) | K250305 | Reprocessed Agilis NxT Steerable Introducer | PNE | 2026-01-07 | View |
| 510(k) | K233825 | Reprocessed Webster Duo-Decapolar Diagnostic EP Catheter | NLH | 2024-06-07 | View |
No matching devices.
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