Sonicision Sterilization Tray

FDA 510(k) K112536 · Covidien

Substantially Equivalent

510(k) numberK112536

Submission

Device name
Sonicision Sterilization Tray
Applicant
Covidien
Boulder, CO, US
Received
September 1, 2011
Decision date
April 19, 2012
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6850
Specialty
General Hospital

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Questions and answers

When was Sonicision Sterilization Tray cleared by the FDA?

Sonicision Sterilization Tray (K112536) received a 510(k) decision of Substantially Equivalent on April 19, 2012, 231 days after the submission was received.

What is the product code of K112536?

The FDA product code is KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, a Class II (moderate risk) device regulated under 21 CFR 880.6850.