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VACPLUS SUCTION UNIT

K103535 Class II Traditional
Decision Date
2011-02-24
Sponsor / Applicant
Apex Medical Corp.

Technical Specification

510(k) Submission ID K103535
Product Code JCX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2011-02-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VACPLUS SUCTION UNIT received FDA 510(k) clearance under submission number K103535, sponsored by Apex Medical 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 2011-02-24.

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.