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STERILE SUREFLEX FILES AND INSTRUMENTS

K971603 Class I Traditional
Decision Date
1997-06-04
Sponsor / Applicant
Dentsply Intl.

Technical Specification

510(k) Submission ID K971603
Product Code EFA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 1997-06-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE SUREFLEX FILES AND INSTRUMENTS received FDA 510(k) clearance under submission number K971603, sponsored by Dentsply Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1997-06-04.

Classification & Regulation

This clearance is catalogued under FDA product code EFA and 21 CFR 872.4200, within the Dental review panel as a Class I device.