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SONICISION STERILIZATION TRAY

K112536 Class II Abbreviated
Decision Date
2012-04-19
Sponsor / Applicant
Covidien

Technical Specification

510(k) Submission ID K112536
Product Code KCT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6850
Decision Date 2012-04-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SONICISION STERILIZATION TRAY received FDA 510(k) clearance under submission number K112536, sponsored by Covidien. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2012-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code KCT and 21 CFR 880.6850, within the General Hospital review panel as a Class II device.