meddevicedb.com FDA Device Reference

Multi-function Platform Systems (BL-M10)

K240474 Class II Traditional
Decision Date
2024-05-20
Sponsor / Applicant
Shanghai Bele Medical Technology Co.,Ltd

Technical Specification

510(k) Submission ID K240474
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 2024-05-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Multi-function Platform Systems (BL-M10) received FDA 510(k) clearance under submission number K240474, sponsored by Shanghai Bele Medical Technology 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 2024-05-20.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.