Last synced on 23 September 2022 at 11:05 pm

MODIFICATION TO CORLINK AUTOMATED ANASTOMOTIC DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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