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D-SIGN I (R&D PROJECT DW263 #24)

K984451 Class II Traditional
Decision Date
1999-01-19
Sponsor / Applicant
Ivoclar North America, Inc.

Technical Specification

510(k) Submission ID K984451
Product Code EJS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3060
Decision Date 1999-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

D-SIGN I (R&D PROJECT DW263 #24) received FDA 510(k) clearance under submission number K984451, sponsored by Ivoclar North America, 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 1999-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code EJS and 21 CFR 872.3060, within the Dental review panel as a Class II device.