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SQ.line KERRISON

Page Type
Cleared 510(K)
510(k) Number
K223596
510(k) Type
Traditional
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2023
Days to Decision
209 days
Submission Type
Summary

SQ.line KERRISON

Page Type
Cleared 510(K)
510(k) Number
K223596
510(k) Type
Traditional
Applicant
Aesculap Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/29/2023
Days to Decision
209 days
Submission Type
Summary