meddevicedb.com FDA Device Reference

CLEAN UP

K922985 Class I Traditional
Decision Date
1993-05-27
Sponsor / Applicant
Bio-Probe, Inc.

Technical Specification

510(k) Submission ID K922985
Product Code EIA
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6640
Decision Date 1993-05-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEAN UP received FDA 510(k) clearance under submission number K922985, sponsored by Bio-Probe, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1993-05-27.

Classification & Regulation

This clearance is catalogued under FDA product code EIA and 21 CFR 872.6640, within the Dental review panel as a Class I device.