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ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K061555
510(k) Type
Traditional
Applicant
ANCHOR PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2006
Days to Decision
87 days
Submission Type
Summary

ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K061555
510(k) Type
Traditional
Applicant
ANCHOR PRODUCTS CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/31/2006
Days to Decision
87 days
Submission Type
Summary