meddevicedb.com FDA Device Reference

1ST IMPRESSION

K921571 Class II Traditional
Decision Date
1993-09-10
Sponsor / Applicant
Wykle Research, Inc.

Technical Specification

510(k) Submission ID K921571
Product Code ELW
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.3660
Decision Date 1993-09-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

1ST IMPRESSION received FDA 510(k) clearance under submission number K921571, sponsored by Wykle Research, 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 1993-09-10.

Classification & Regulation

This clearance is catalogued under FDA product code ELW and 21 CFR 872.3660, within the Dental review panel as a Class II device.