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RUBBER LATEX SURGICAL GLOVES, STERILE

K895448 Class I Traditional
Decision Date
1989-10-10
Sponsor / Applicant
Dah Lee Rubber Industries (Thai) , Ltd.

Technical Specification

510(k) Submission ID K895448
Product Code KGO
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4460
Decision Date 1989-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RUBBER LATEX SURGICAL GLOVES, STERILE received FDA 510(k) clearance under submission number K895448, sponsored by Dah Lee Rubber Industries (Thai) , Ltd.. 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 1989-10-10.

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.