meddevicedb.com FDA Device Reference

G.o.c.c.l.e.s.

K151630 Class II Traditional
Decision Date
2015-09-15
Sponsor / Applicant
Pierrel Pharma S.R.L.

Technical Specification

510(k) Submission ID K151630
Product Code NXV
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6350
Decision Date 2015-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

G.o.c.c.l.e.s. received FDA 510(k) clearance under submission number K151630, sponsored by Pierrel Pharma S.R.L.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2015-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code NXV and 21 CFR 872.6350, within the Dental review panel as a Class II device.