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V5MS TRANSDUCER AND MPT7-4 MULTIPLANE TRANSESOPHAGEAL TRANSDUCER

K052021 Class II Special
Decision Date
2005-08-17
Sponsor / Applicant
Siemens Medical Solutions USA, Inc.

Technical Specification

510(k) Submission ID K052021
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 2005-08-17
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V5MS TRANSDUCER AND MPT7-4 MULTIPLANE TRANSESOPHAGEAL TRANSDUCER received FDA 510(k) clearance under submission number K052021, sponsored by Siemens Medical Solutions USA, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2005-08-17.

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.