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OPTICROSS 40 MHZ CORONARY IMAGING CATHETER

K123621 Class II Traditional
Decision Date
2013-04-15
Sponsor / Applicant
Boston Scientific Corp

Technical Specification

510(k) Submission ID K123621
Product Code OBJ
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2013-04-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OPTICROSS 40 MHZ CORONARY IMAGING CATHETER received FDA 510(k) clearance under submission number K123621, 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 2013-04-15.

Classification & Regulation

This clearance is catalogued under FDA product code OBJ and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.