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SPECTRA (ULTRAVIOLET PRODUCTS)

Page Type
Cleared 510(K)
510(k) Number
K827123
510(k) Type
Traditional
Applicant
ULTRALITE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1982
Days to Decision
31 days

SPECTRA (ULTRAVIOLET PRODUCTS)

Page Type
Cleared 510(K)
510(k) Number
K827123
510(k) Type
Traditional
Applicant
ULTRALITE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/5/1982
Days to Decision
31 days