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CORNEAL SCLERAL LANCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840855
510(k) Type
Traditional
Applicant
SHARPOINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1984
Days to Decision
75 days

CORNEAL SCLERAL LANCE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840855
510(k) Type
Traditional
Applicant
SHARPOINT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/9/1984
Days to Decision
75 days