meddevicedb.com FDA Device Reference

PM POSITIONER

K953293 Class II Traditional
Decision Date
1995-09-15
Sponsor / Applicant
Jonathan A. Parker, D.D.S.

Technical Specification

510(k) Submission ID K953293
Product Code LQZ
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5570
Decision Date 1995-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PM POSITIONER received FDA 510(k) clearance under submission number K953293, sponsored by Jonathan A. Parker, D.D.S.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1995-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code LQZ and 21 CFR 872.5570, within the Dental review panel as a Class II device.