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WINGMAN EXTENDABLE TIP SUPPORT CATHETER

K120178 Class II Special
Decision Date
2012-02-08
Sponsor / Applicant
Reflow Medical

Technical Specification

510(k) Submission ID K120178
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2012-02-08
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WINGMAN EXTENDABLE TIP SUPPORT CATHETER received FDA 510(k) clearance under submission number K120178, sponsored by Reflow Medical. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2012-02-08.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.