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AESCULAP VENTRICULOSCOPE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K954394
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
171 days
Submission Type
Summary

AESCULAP VENTRICULOSCOPE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K954394
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/7/1996
Days to Decision
171 days
Submission Type
Summary