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Suntan Lamp
FDA product code REG · Class 2 · General, Plastic Surgery
0
Registered devices
2
Adverse events
1
Recalls
0
510(k) clearances
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-09-08 | Solafeet, Inc. | Product failed to have a label that contained a recommended exposure schedule; the operator's manual provided inadequate instructions for use; and label implica |
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