Lunar Radiation Corp.
FDA 510(k) & PMA Approved Devices — 6 products
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Total Devices6
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K873296 | DPX BONE DENSITOMETER | KGI | 1988-06-06 | View |
| 510(k) | K810159 | BONE MINERAL ANALYZER CONTROLLER | KGI | 1981-02-12 | View |
| 510(k) | K810140 | DUAL-PHOTON TOTAL BODY BONE MINERAL ANA | KGI | 1981-02-12 | View |
| 510(k) | K802180 | WISCONSIN DUAL-PHOTON BONE ANALYZER | KGI | 1980-12-31 | View |
| 510(k) | K802181 | WISCONSIN BONE MINERAL ANALYZER | KGI | 1980-12-31 | View |
| 510(k) | K802182 | WISCONSIN HEART RATE MONITOR | DRT | 1980-10-31 | View |
No matching devices.
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