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HOUVA-LITE PALM UNIT #501

K761188 Class II Traditional
Decision Date
1977-02-28
Sponsor / Applicant
National Biological Corp.

Technical Specification

510(k) Submission ID K761188
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 PALM UNIT #501 received FDA 510(k) clearance under submission number K761188, 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.