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MEGABEAM ENDOCULAR PROBE

Page Type
Cleared 510(K)
510(k) Number
K935747
510(k) Type
Traditional
Applicant
CERAMOPTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1994
Days to Decision
121 days
Submission Type
Summary

MEGABEAM ENDOCULAR PROBE

Page Type
Cleared 510(K)
510(k) Number
K935747
510(k) Type
Traditional
Applicant
CERAMOPTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/1994
Days to Decision
121 days
Submission Type
Summary