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DLR-1 DERMA-LASE RUBY LASER/DLR-1/DERMA-LASE SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924647
510(k) Type
Traditional
Applicant
DERMA-LASE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1993
Days to Decision
263 days
Submission Type
Statement

DLR-1 DERMA-LASE RUBY LASER/DLR-1/DERMA-LASE SYST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924647
510(k) Type
Traditional
Applicant
DERMA-LASE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/1993
Days to Decision
263 days
Submission Type
Statement