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50S TRINGA ULTRASOUND IMAGING SYSTEM

K020112 Class II Traditional
Decision Date
2002-04-19
Sponsor / Applicant
Pie Medical

Technical Specification

510(k) Submission ID K020112
Product Code IYO
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1560
Decision Date 2002-04-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

50S TRINGA ULTRASOUND IMAGING SYSTEM received FDA 510(k) clearance under submission number K020112, sponsored by Pie Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2002-04-19.

Classification & Regulation

This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.