meddevicedb.com FDA Device Reference

COVER UP

K881914 Class II Traditional
Decision Date
1988-07-15
Sponsor / Applicant
Parkell

Technical Specification

510(k) Submission ID K881914
Product Code EMA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3275
Decision Date 1988-07-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COVER UP received FDA 510(k) clearance under submission number K881914, sponsored by Parkell. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1988-07-15.

Classification & Regulation

This clearance is catalogued under FDA product code EMA and 21 CFR 872.3275, within the Dental review panel as a Class II device.