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COOL-TIP RF GENERATOR, COOL-TIP RF SYSTEM ACCESSORIES

K053290 Class II Traditional
Decision Date
2006-03-15
Sponsor / Applicant
Valleylab

Technical Specification

510(k) Submission ID K053290
Product Code GEI
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4400
Decision Date 2006-03-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COOL-TIP RF GENERATOR, COOL-TIP RF SYSTEM ACCESSORIES received FDA 510(k) clearance under submission number K053290, sponsored by Valleylab. 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 2006-03-15.

Classification & Regulation

This clearance is catalogued under FDA product code GEI and 21 CFR 878.4400, within the General, Plastic Surgery review panel as a Class II device.