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ENDOS AC/ACP

K030185 Class II Abbreviated
Decision Date
2003-03-11
Sponsor / Applicant
Villa Sistemi Medicali S.P.A.

Technical Specification

510(k) Submission ID K030185
Product Code EHD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2003-03-11
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ENDOS AC/ACP received FDA 510(k) clearance under submission number K030185, sponsored by Villa Sistemi Medicali S.P.A.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2003-03-11.

Classification & Regulation

This clearance is catalogued under FDA product code EHD and 21 CFR 872.1800, within the Dental review panel as a Class II device.