meddevicedb.com FDA Device Reference

Vas-Q-Clip

K151943 Class II Traditional
Decision Date
2016-03-25
Sponsor / Applicant
Nanova Biomaterials, Inc.

Technical Specification

510(k) Submission ID K151943
Product Code FZP
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4300
Decision Date 2016-03-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Vas-Q-Clip received FDA 510(k) clearance under submission number K151943, sponsored by Nanova Biomaterials, Inc.. 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 2016-03-25.

Classification & Regulation

This clearance is catalogued under FDA product code FZP and 21 CFR 878.4300, within the General, Plastic Surgery review panel as a Class II device.