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DENTA SAFE(TM) LATEX EXAMINATION GLOVES

K912999 Class I Traditional
Decision Date
1991-08-13
Sponsor / Applicant
Dental Care Intl., Inc.

Technical Specification

510(k) Submission ID K912999
Product Code LYY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6250
Decision Date 1991-08-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTA SAFE(TM) LATEX EXAMINATION GLOVES received FDA 510(k) clearance under submission number K912999, sponsored by Dental Care Intl., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1991-08-13.

Classification & Regulation

This clearance is catalogued under FDA product code LYY and 21 CFR 880.6250, within the General Hospital review panel as a Class I device.