Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted 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
FDA Hosted 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