Last synced on 25 January 2026 at 3:41 am

SONICISION CORDLESS ULTRASONIC DISSECTION DEVICE MODEL SCD391, SCD396, SCT12, SCG, SCB, SCSK, SONICISION STERILIZATION T

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101797
510(k) Type
Traditional
Applicant
Covidien, Formerly Valleylab, A Division of Tyco
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2011
Days to Decision
241 days
Submission Type
Summary

SONICISION CORDLESS ULTRASONIC DISSECTION DEVICE MODEL SCD391, SCD396, SCT12, SCG, SCB, SCSK, SONICISION STERILIZATION T

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K101797
510(k) Type
Traditional
Applicant
Covidien, Formerly Valleylab, A Division of Tyco
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/24/2011
Days to Decision
241 days
Submission Type
Summary