meddevicedb.com FDA Device Reference

ULTRASONIC IMAGING CATHETER

K883202 Class II Traditional
Decision Date
1988-11-23
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K883202
Product Code DXO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2870
Decision Date 1988-11-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ULTRASONIC IMAGING CATHETER received FDA 510(k) clearance under submission number K883202, sponsored by Boston Scientific Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1988-11-23.

Classification & Regulation

This clearance is catalogued under FDA product code DXO and 21 CFR 870.2870, within the Cardiovascular review panel as a Class II device.