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PANA SPRAY PLUS

K131014 Class I Traditional
Decision Date
2013-08-12
Sponsor / Applicant
Nsk America Corp.

Technical Specification

510(k) Submission ID K131014
Product Code EFB
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4200
Decision Date 2013-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PANA SPRAY PLUS received FDA 510(k) clearance under submission number K131014, sponsored by Nsk America Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2013-08-12.

Classification & Regulation

This clearance is catalogued under FDA product code EFB and 21 CFR 872.4200, within the Dental review panel as a Class I device.