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SHARPLAN 2100 ND:YAG LASER, SERIES 2900 SYN. TIPS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883563
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1988
Days to Decision
39 days

SHARPLAN 2100 ND:YAG LASER, SERIES 2900 SYN. TIPS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K883563
510(k) Type
Traditional
Applicant
SHARPLAN LASERS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/1988
Days to Decision
39 days