Gold Coast Imaging, 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) | K933430 | CYTOGUIDE STEREOTATIC BIOPSY SYSTEM | IZH | 1994-09-22 | View |
| 510(k) | K925212 | GIOTTO PATIENT BED | IZH | 1993-01-15 | View |
No matching devices.
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