Uti-Tect, 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) | K840160 | B-STREP-TECT-II | JSI | 1984-03-02 | View |
| 510(k) | K840159 | GC-TECT | JTY | 1984-01-30 | View |
| 510(k) | K812581 | SENSI-TECT | JTZ | 1981-09-23 | View |
No matching devices.
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