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IMPREGUM PENTA M MONOSOFT

K994192 Class II Traditional
Decision Date
2000-01-28
Sponsor / Applicant
Espe Dental AG

Technical Specification

510(k) Submission ID K994192
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 2000-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IMPREGUM PENTA M MONOSOFT received FDA 510(k) clearance under submission number K994192, sponsored by Espe Dental AG. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2000-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.