meddevicedb.com FDA Device Reference

SMARTSUCTION HARMONY DEVICE

K052626 Class II Traditional
Decision Date
2005-10-05
Sponsor / Applicant
Haemonetics Corp.

Technical Specification

510(k) Submission ID K052626
Product Code BTA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2005-10-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SMARTSUCTION HARMONY DEVICE received FDA 510(k) clearance under submission number K052626, sponsored by Haemonetics Corp.. 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 2005-10-05.

Classification & Regulation

This clearance is catalogued under FDA product code BTA and 21 CFR 878.4780, within the General, Plastic Surgery review panel as a Class II device.