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RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122781
510(k) Type
Traditional
Applicant
COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2013
Days to Decision
147 days
Submission Type
Summary

RELIAMAX GASTROINTESTINAL ANASTOMOSIS AND RELOAD

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122781
510(k) Type
Traditional
Applicant
COVIDIEN, FORMERLY US SURGICAL A DIVISON OF TYCO H
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2013
Days to Decision
147 days
Submission Type
Summary