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MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K020470
510(k) Type
Special
Applicant
BYPASS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2002
Days to Decision
24 days
Submission Type
Summary

MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE

Page Type
Cleared 510(K)
510(k) Number
K020470
510(k) Type
Special
Applicant
BYPASS LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2002
Days to Decision
24 days
Submission Type
Summary