meddevicedb.com FDA Device Reference

CARE SU01A SUCTION ASPIRATOR

K130001 Class II Traditional
Decision Date
2013-07-25
Sponsor / Applicant
Foshan Care Medical Technology Co., Ltd.

Technical Specification

510(k) Submission ID K130001
Product Code JCX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2013-07-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARE SU01A SUCTION ASPIRATOR received FDA 510(k) clearance under submission number K130001, sponsored by Foshan Care 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 2013-07-25.

Classification & Regulation

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