meddevicedb.com FDA Device Reference

DENTANURSE

K891607 Class II Traditional
Decision Date
1989-08-11
Sponsor / Applicant
The Irish Scene

Technical Specification

510(k) Submission ID K891607
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 1989-08-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTANURSE received FDA 510(k) clearance under submission number K891607, sponsored by The Irish Scene. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1989-08-11.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.