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Osram GmbH

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K863937OSRAM ULTRAMED 400 WNovember 4, 1986
K812853OSRAM UVA LAMPDecember 9, 1981