meddevicedb.com FDA Device Reference

LIQUIDBAND FLOW CONTROL

K122446 Class II Traditional
Decision Date
2012-10-26
Sponsor / Applicant
Advanced Medical Solutions (Plymouth), Ltd.

Technical Specification

510(k) Submission ID K122446
Product Code MPN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4010
Decision Date 2012-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIQUIDBAND FLOW CONTROL received FDA 510(k) clearance under submission number K122446, sponsored by Advanced Medical Solutions (Plymouth), Ltd.. 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 2012-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code MPN and 21 CFR 878.4010, within the General, Plastic Surgery review panel as a Class II device.