Last synced on 14 November 2025 at 11:06 pm

Aesculap Aicon® Series Container System

Page Type
Cleared 510(K)
510(k) Number
K242762
510(k) Type
Traditional
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2025
Days to Decision
243 days
Submission Type
Summary

Aesculap Aicon® Series Container System

Page Type
Cleared 510(K)
510(k) Number
K242762
510(k) Type
Traditional
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/13/2025
Days to Decision
243 days
Submission Type
Summary