meddevicedb.com FDA Device Reference

Suction Pump (SU-90)

K260892 Class II Traditional
Decision Date
2026-05-14
Sponsor / Applicant
Shenzhen HugeMed Medical Technical Development Co., Ltd.

Technical Specification

510(k) Submission ID K260892
Product Code BTA
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2026-05-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Suction Pump (SU-90) received FDA 510(k) clearance under submission number K260892, sponsored by Shenzhen HugeMed Medical Technical Development Co., 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 2026-05-14.

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.