meddevicedb.com FDA Device Reference

Cross Wise™ Multi-Use RF Adapter Cable

K243193 Class II Special
Decision Date
2024-11-26
Sponsor / Applicant
Circa Scientific, Inc.

Technical Specification

510(k) Submission ID K243193
Product Code DXF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5175
Decision Date 2024-11-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Cross Wise™ Multi-Use RF Adapter Cable received FDA 510(k) clearance under submission number K243193, sponsored by Circa Scientific, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-11-26.

Classification & Regulation

This clearance is catalogued under FDA product code DXF and 21 CFR 870.5175, within the Cardiovascular review panel as a Class II device.