meddevicedb.com FDA Device Reference

Finessis Zero Flexylon Powder Free Sterile White Surgical Glove

K171987 Class I Special
Decision Date
2017-10-20
Sponsor / Applicant
Lucenxia Prescience AG

Technical Specification

510(k) Submission ID K171987
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 2017-10-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Finessis Zero Flexylon Powder Free Sterile White Surgical Glove received FDA 510(k) clearance under submission number K171987, sponsored by Lucenxia Prescience AG. The device was reviewed via the Special premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 2017-10-20.

Classification & Regulation

This clearance is catalogued under FDA product code KGO and 21 CFR 878.4460, within the General, Plastic Surgery review panel as a Class I device.