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GUTTA PERCHA POINTS

K863638 Class I Traditional
Decision Date
1986-10-30
Sponsor / Applicant
Endodent, Inc.

Technical Specification

510(k) Submission ID K863638
Product Code EKM
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3850
Decision Date 1986-10-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GUTTA PERCHA POINTS received FDA 510(k) clearance under submission number K863638, sponsored by Endodent, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1986-10-30.

Classification & Regulation

This clearance is catalogued under FDA product code EKM and 21 CFR 872.3850, within the Dental review panel as a Class I device.