Krupp International, 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) | K800835 | KANDI-NUCLEAR MED. DATA ACQU.&INFO. | 1980-05-28 | View | |
| 510(k) | K780090 | DENTAL ALLOY | EJH | 1978-03-14 | View |
No matching devices.
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