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DERMA-LASE RUBY LASER - MODEL DLR-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913256
510(k) Type
Traditional
Applicant
DERMA-LASE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1992
Days to Decision
190 days
Submission Type
Statement

DERMA-LASE RUBY LASER - MODEL DLR-1

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K913256
510(k) Type
Traditional
Applicant
DERMA-LASE CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/1992
Days to Decision
190 days
Submission Type
Statement