meddevicedb.com FDA Device Reference

R&D Series Nova Compo-B Plus Bottle, R&D Series Nova Compo-B Plus Single Dose

K192913 Class II Traditional
Decision Date
2021-01-19
Sponsor / Applicant
Imicryl Dis Malzemeleri Sanayi VE Ticaret AS

Technical Specification

510(k) Submission ID K192913
Product Code KLE
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3200
Decision Date 2021-01-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

R&D Series Nova Compo-B Plus Bottle, R&D Series Nova Compo-B Plus Single Dose received FDA 510(k) clearance under submission number K192913, sponsored by Imicryl Dis Malzemeleri Sanayi VE Ticaret AS. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2021-01-19.

Classification & Regulation

This clearance is catalogued under FDA product code KLE and 21 CFR 872.3200, within the Dental review panel as a Class II device.