Medron, Inc.
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) | K971897 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH) | LFK | 1997-10-21 | View |
| 510(k) | K940775 | INJECTION CAP | FOZ | 1994-06-15 | View |
No matching devices.
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