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SHARPLAN 2100,3000,SHARPLASER 65, 40

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920865
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1993
Days to Decision
524 days
Submission Type
Summary

SHARPLAN 2100,3000,SHARPLASER 65, 40

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920865
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/2/1993
Days to Decision
524 days
Submission Type
Summary