meddevicedb.com FDA Device Reference

LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES

K981172 Class II Traditional
Decision Date
1998-06-30
Sponsor / Applicant
Byron Medical

Technical Specification

510(k) Submission ID K981172
Product Code QPB
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5040
Decision Date 1998-06-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LIPOPLASTY/ LIPOSUCTION ASPIRATION AND TUMESCENT INFUSION CANNULAE AND NEEDLES received FDA 510(k) clearance under submission number K981172, sponsored by Byron Medical. 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 1998-06-30.

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.