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MEGABEAM ENDO-ENT PROBE

Page Type
Cleared 510(K)
510(k) Number
K952772
510(k) Type
Traditional
Applicant
CERAMOPTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1995
Days to Decision
31 days
Submission Type
Summary

MEGABEAM ENDO-ENT PROBE

Page Type
Cleared 510(K)
510(k) Number
K952772
510(k) Type
Traditional
Applicant
CERAMOPTEC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/17/1995
Days to Decision
31 days
Submission Type
Summary