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RECRUIT MICROCATHETER

K091563 Class II Traditional
Decision Date
2009-07-30
Sponsor / Applicant
Reverse Medical Corporation

Technical Specification

510(k) Submission ID K091563
Product Code MMX
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5150
Decision Date 2009-07-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RECRUIT MICROCATHETER received FDA 510(k) clearance under submission number K091563, sponsored by Reverse Medical Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-07-30.

Classification & Regulation

This clearance is catalogued under FDA product code MMX and 21 CFR 870.5150, within the Cardiovascular review panel as a Class II device.