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Reprocessed Covidien LigaSure 5mm, Blunt Tip, Laparoscopic Sealer/Divider

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143260
510(k) Type
Traditional
Applicant
Sterilmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2015
Days to Decision
102 days
Submission Type
Summary

Reprocessed Covidien LigaSure 5mm, Blunt Tip, Laparoscopic Sealer/Divider

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143260
510(k) Type
Traditional
Applicant
Sterilmed, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2015
Days to Decision
102 days
Submission Type
Summary