Catheter Precision, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2020-09-14
SEC Filings: 1 filings on record. Latest: 8-K (2026-05-18). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200313 | VIVO | DQK | 2020-09-14 | View |
| 510(k) | K183195 | VIVO | DQK | 2019-06-14 | View |
No matching devices.