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Solitec GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K903660DERMALIGHT PSORACOMBJuly 17, 1991
K828671UVATEC SUNTAMED 4000 AND 2000January 19, 1983
K828670UVATEC SUNTAMED 400January 17, 1983