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Paul B. Elder Co.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K810358
PHOTOTHERAPY LIGHT CHAMBER
March 20, 1981
K791977
PSORALITE MARK I
December 28, 1979
K791116
PSORALITE SERIES 30,000
September 4, 1979