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OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDE

Page Type
Cleared 510(K)
510(k) Number
K853598
510(k) Type
Traditional
Applicant
MYOCURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1985
Days to Decision
69 days

OPHTHALMIC KNIFE W/REMOVALE DEPTH GUIDE

Page Type
Cleared 510(K)
510(k) Number
K853598
510(k) Type
Traditional
Applicant
MYOCURE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/4/1985
Days to Decision
69 days