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PANOSOL II TRU-BLU, MODEL UBL-417

K070934 Class II Traditional
Decision Date
2007-05-22
Sponsor / Applicant
National Biological Corp.

Technical Specification

510(k) Submission ID K070934
Product Code FTC
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4630
Decision Date 2007-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PANOSOL II TRU-BLU, MODEL UBL-417 received FDA 510(k) clearance under submission number K070934, 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 2007-05-22.

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.