Medcraft Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K860467 | ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 | QGH | 1986-11-10 | View |
| 510(k) | K791795 | COMP-ACT IV | DPS | 1979-09-27 | View |
| 510(k) | K760510 | MONITORING SYSTEM, REHABILITATION | DPS | 1976-08-30 | View |
| 510(k) | K760509 | TREADMILL, DIAGNOSTIC | IOL | 1976-08-30 | View |
| 510(k) | K760508 | ACCUTAPE 24 | DSH | 1976-08-30 | View |
No matching devices.
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