meddevicedb.com FDA Device Reference

PET-512MC TRANSESOPHAGEAL TRANSDUCER

K103629 Class II Traditional
Decision Date
2011-02-02
Sponsor / Applicant
Toshiba America Medical Systems, In.C

Technical Specification

510(k) Submission ID K103629
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2011-02-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PET-512MC TRANSESOPHAGEAL TRANSDUCER received FDA 510(k) clearance under submission number K103629, sponsored by Toshiba America Medical Systems, In.C. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2011-02-02.

Classification & Regulation

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