meddevicedb.com FDA Device Reference

ISODYNE

K770558 Class I Traditional
Decision Date
1977-04-05
Sponsor / Applicant
Hmw Industries

Technical Specification

510(k) Submission ID K770558
Product Code ECO
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.5410
Decision Date 1977-04-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ISODYNE received FDA 510(k) clearance under submission number K770558, sponsored by Hmw Industries. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1977-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code ECO and 21 CFR 872.5410, within the Dental review panel as a Class I device.