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SAFETYWAND DISPOSABLE HANDPIECE

K023722 Class II Traditional
Decision Date
2003-09-02
Sponsor / Applicant
Spintech, Inc.

Technical Specification

510(k) Submission ID K023722
Product Code EJI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6770
Decision Date 2003-09-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SAFETYWAND DISPOSABLE HANDPIECE received FDA 510(k) clearance under submission number K023722, sponsored by Spintech, 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 2003-09-02.

Classification & Regulation

This clearance is catalogued under FDA product code EJI and 21 CFR 872.6770, within the Dental review panel as a Class II device.