meddevicedb.com FDA Device Reference

VCARE A

K121817 Class II Traditional
Decision Date
2013-09-17
Sponsor / Applicant
IVT Medical, Ltd.

Technical Specification

510(k) Submission ID K121817
Product Code OMP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4780
Decision Date 2013-09-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VCARE A received FDA 510(k) clearance under submission number K121817, sponsored by IVT Medical, 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 2013-09-17.

Classification & Regulation

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