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AESCULAP LAPAROSCOPIC ANCILLARY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K943603
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1995
Days to Decision
247 days
Submission Type
Summary

AESCULAP LAPAROSCOPIC ANCILLARY DEVICES

Page Type
Cleared 510(K)
510(k) Number
K943603
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/1995
Days to Decision
247 days
Submission Type
Summary