Clareblend, 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) | K073000 | LUMAPROBE | GEX | 2008-10-01 | View |
| 510(k) | K073022 | CLAREBLEND LED PROBES MODEL# 7201-415, 7204-631, 7205-830 | GEX | 2008-10-01 | View |
| 510(k) | K880553 | ELECTRONIC EPILATOR | KCW | 1988-02-29 | View |
No matching devices.
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