Baylis Medical Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
Total Devices5
Categories3
Latest Approval2026-01-18
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K254114 | Baylis Connector Cable | DSA | 2026-01-18 | View |
| 510(k) | K250275 | PrecisePath Radiofrequency Puncture Generator and PrecisePath Footswitch | GEI | 2025-10-28 | View |
| 510(k) | K251158 | PowerWire® 14 Radiofrequency Guidewire Kit | PDU | 2025-09-11 | View |
| 510(k) | K232562 | PowerWire Radiofrequency Guidewire Kit | PDU | 2024-02-28 | View |
| 510(k) | K230571 | RFP-100A Connector Cable (Single Use) | DSA | 2023-05-30 | View |
No matching devices.