Mecta Corp.
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) | K965070 | SPECTRUM 5000 Q, 5000Q,M,4000 Q, 4000 M. | QGH | 1997-03-06 | View |
| 510(k) | K960754 | SPECTRUM 5000 Q, 5000 M, 4000 Q, 4000 M | QGH | 1996-09-18 | View |
| 510(k) | K852069 | MECTA ECT DEVICE MODELS SR & JR | QGH | 1985-08-09 | View |
No matching devices.
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