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Waldmann Lighting Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
2
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K053364
HALUX IRIS EXAMINATION AND SURGICAL LAMP
February 23, 2006
K841795
UV 8001K, PUVA 800, PUVA 180/200 1000
August 30, 1984