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THIXO-GEL ULTRASOUND SPRAY

K121311 Class II Traditional
Decision Date
2012-08-30
Sponsor / Applicant
Cloverline International Pharma Services GmbH

Technical Specification

510(k) Submission ID K121311
Product Code MUI
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2012-08-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THIXO-GEL ULTRASOUND SPRAY received FDA 510(k) clearance under submission number K121311, sponsored by Cloverline International Pharma Services GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2012-08-30.

Classification & Regulation

This clearance is catalogued under FDA product code MUI and 21 CFR 892.1570, within the Radiology review panel as a Class II device.