Houston Biomedical, 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) | K861291 | GASTROTOPO | FGE | 1987-05-15 | View |
| 510(k) | K861241 | ANGIOTOPO CATHETER | DQO | 1987-01-06 | View |
| 510(k) | K861200 | UROTOPO CATHETER | KOD | 1986-04-23 | View |
No matching devices.
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