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AESCULAP RIGID ENDOSCOPES

Page Type
Cleared 510(K)
510(k) Number
K933834
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1993
Days to Decision
137 days
Submission Type
Summary

AESCULAP RIGID ENDOSCOPES

Page Type
Cleared 510(K)
510(k) Number
K933834
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1993
Days to Decision
137 days
Submission Type
Summary