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SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)

Page Type
Cleared 510(K)
510(k) Number
K971874
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1997
Days to Decision
90 days
Submission Type
Summary

SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)

Page Type
Cleared 510(K)
510(k) Number
K971874
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1997
Days to Decision
90 days
Submission Type
Summary