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Aesculap Caiman 12 Seal and Cut Technology System

Page Type
Cleared 510(K)
510(k) Number
K203461
510(k) Type
Special
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2020
Days to Decision
24 days
Submission Type
Summary

Aesculap Caiman 12 Seal and Cut Technology System

Page Type
Cleared 510(K)
510(k) Number
K203461
510(k) Type
Special
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2020
Days to Decision
24 days
Submission Type
Summary