meddevicedb.com FDA Device Reference

HOUVA-LITE ARM UNIT #601

K761186 Class II Traditional
Decision Date
1977-02-28
Sponsor / Applicant
National Biological Corp.

Technical Specification

510(k) Submission ID K761186
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 1977-02-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOUVA-LITE ARM UNIT #601 received FDA 510(k) clearance under submission number K761186, sponsored by National Biological Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1977-02-28.

Classification & Regulation

This clearance is catalogued under FDA product code FTC and 21 CFR 878.4630, within the General, Plastic Surgery review panel as a Class II device.