meddevicedb.com FDA Device Reference

DENTAL PIK

K892861 Class I Traditional
Decision Date
1989-09-15
Sponsor / Applicant
U.S. Dentek Corp.

Technical Specification

510(k) Submission ID K892861
Product Code EKS
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1989-09-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DENTAL PIK received FDA 510(k) clearance under submission number K892861, sponsored by U.S. Dentek 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 1989-09-15.

Classification & Regulation

This clearance is catalogued under FDA product code EKS and 21 CFR 872.4565, within the Dental review panel as a Class I device.