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MULTI-PULSE 2000

K001248 Class II Traditional
Decision Date
2000-05-04
Sponsor / Applicant
Imaging Sciences Intl., Inc.

Technical Specification

510(k) Submission ID K001248
Product Code EHD
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.1800
Decision Date 2000-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MULTI-PULSE 2000 received FDA 510(k) clearance under submission number K001248, sponsored by Imaging Sciences Intl., 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 2000-05-04.

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.