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Ultralite

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K910091ULTRALITE PANELITEMay 30, 1991
K861963ULTRALITE HF1236 HAND AND FOOT SYSTEMJune 25, 1986
K820492SPECTRA305March 31, 1982
K827123SPECTRA (ULTRAVIOLET PRODUCTS)March 5, 1982
K820280SPECTRA 305/350March 5, 1982
K761179PSORALITEMay 3, 1977