Artemis Medical, Inc.
FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K032217 | 14G CORMARK BIOPSY SITE IDENTIFIER | FZP | 2003-08-21 | View |
| 510(k) | K020024 | CARIS MINITOME BIOPSY INSTRUMENT | KNW | 2002-04-03 | View |
| 510(k) | K003777 | CARIS SITE MARKER | FZP | 2001-03-06 | View |
No matching devices.
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