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CIMPAT

K830109 Class I Traditional
Decision Date
1983-03-01
Sponsor / Applicant
North Pacific Dental, Inc.

Technical Specification

510(k) Submission ID K830109
Product Code EMR
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1983-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CIMPAT received FDA 510(k) clearance under submission number K830109, sponsored by North Pacific Dental, 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 1983-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code EMR and 21 CFR 872.4565, within the Dental review panel as a Class I device.