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ELASTYREN POWDER-FREE SURGICAL GLOVE

K971471 Class I Traditional
Decision Date
1998-02-09
Sponsor / Applicant
Eci Medical Technologies, Inc.

Technical Specification

510(k) Submission ID K971471
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1998-02-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELASTYREN POWDER-FREE SURGICAL GLOVE received FDA 510(k) clearance under submission number K971471, 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 1998-02-09.

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.