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DERMALIGHT SPOT

Page Type
Cleared 510(K)
510(k) Number
K828676
510(k) Type
Traditional
Applicant
DR. K. HONLE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1983
Days to Decision
48 days

DERMALIGHT SPOT

Page Type
Cleared 510(K)
510(k) Number
K828676
510(k) Type
Traditional
Applicant
DR. K. HONLE GMBH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1983
Days to Decision
48 days