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Aesculap AICON Container

Page Type
Cleared 510(K)
510(k) Number
K214041
510(k) Type
Traditional
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2022
Days to Decision
372 days
Submission Type
Summary

Aesculap AICON Container

Page Type
Cleared 510(K)
510(k) Number
K214041
510(k) Type
Traditional
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/30/2022
Days to Decision
372 days
Submission Type
Summary