Digisonics, 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) | K970402 | DOCTORS REVIEW SYSTEM | LLZ | 1997-03-26 | View |
| 510(k) | K900271 | MODEL OB-500 FETAL GROWTH ANALYSIS & OPTION OBLINK | HEM | 1990-04-19 | View |
| 510(k) | K800766 | ECHO-COMP | DQK | 1980-04-24 | View |
No matching devices.
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