meddevicedb.com FDA Device Reference

ELASTYREN(R) SURGICAL GLOVES

K945833 Class I Traditional
Decision Date
1995-01-17
Sponsor / Applicant
Eci Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K945833
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1995-01-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELASTYREN(R) SURGICAL GLOVES received FDA 510(k) clearance under submission number K945833, sponsored by Eci Medical Technologies, 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 1995-01-17.

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.