Opko Health, Inc.
FDA 510(k) & PMA Approved Devices — 1 products
Total Devices1
Categories1
Latest FDA decision2025-07-25
SEC Filings: 1 filings on record. Latest: 10-Q/A (2026-08-28). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| PMA | P190022 | Multi-analyte test system with algorithmic analysis for detection of prostate cancer | QRF | 2025-07-25 | View |
No matching devices.