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DIAGNOSTIC ULTRASOUND IMAGING CATHETER

K940108 Class II Traditional
Decision Date
1994-12-07
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K940108
Product Code ITX
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1570
Decision Date 1994-12-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAGNOSTIC ULTRASOUND IMAGING CATHETER received FDA 510(k) clearance under submission number K940108, sponsored by Boston Scientific Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 1994-12-07.

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.