Medspira, LLC
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) | K252605 | mcompass Anorectal Balloon Expulsion Catheter (RMD-003-001) | FFX | 2025-12-05 | View |
| 510(k) | K120088 | MCOMPASS ANORECTAL MANOMETRY SYSTEM | KLA | 2012-03-29 | View |
No matching devices.
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