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AESCULAP PRIMELINE CONTAINER LTD.

Page Type
Cleared 510(K)
510(k) Number
K073168
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2008
Days to Decision
171 days
Submission Type
Summary

AESCULAP PRIMELINE CONTAINER LTD.

Page Type
Cleared 510(K)
510(k) Number
K073168
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/28/2008
Days to Decision
171 days
Submission Type
Summary