meddevicedb.com FDA Device Reference

ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA

K932664 Class I Traditional
Decision Date
1993-12-22
Sponsor / Applicant
Smith & Nephew Perry

Technical Specification

510(k) Submission ID K932664
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1993-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA received FDA 510(k) clearance under submission number K932664, sponsored by Smith & Nephew Perry. 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 1993-12-22.

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.