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AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY

Page Type
Cleared 510(K)
510(k) Number
K010752
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2001
Days to Decision
90 days
Submission Type
Summary

AESCULAP'S MODULAR ENDOSCOPIC INSTRUMENTS FOR GYNECOLOGY

Page Type
Cleared 510(K)
510(k) Number
K010752
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/2001
Days to Decision
90 days
Submission Type
Summary