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UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931774
510(k) Type
Traditional
Applicant
SUNRISE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
104 days
Submission Type
Summary

UPGRADED PACKAGE FOR DLASE 300 PULSED DENTAL LASER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931774
510(k) Type
Traditional
Applicant
SUNRISE TECHNOLOGIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/22/1993
Days to Decision
104 days
Submission Type
Summary