meddevicedb.com FDA Device Reference

SORING GMBH SONOCA LIPO

K052183 Class II Traditional
Decision Date
2005-10-07
Sponsor / Applicant
Soring GmbH Medizintechnik

Technical Specification

510(k) Submission ID K052183
Product Code QPB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5040
Decision Date 2005-10-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SORING GMBH SONOCA LIPO received FDA 510(k) clearance under submission number K052183, sponsored by Soring GmbH Medizintechnik. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2005-10-07.

Classification & Regulation

This clearance is catalogued under FDA product code QPB and 21 CFR 878.5040, within the General, Plastic Surgery review panel as a Class II device.