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MERIT MAK (MINI ACCESS KIT) WITH PALLADIUM TIP GUIDE WIRE

K091584 Class II Traditional
Decision Date
2009-10-09
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K091584
Product Code DRE
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1310
Decision Date 2009-10-09
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MERIT MAK (MINI ACCESS KIT) WITH PALLADIUM TIP GUIDE WIRE received FDA 510(k) clearance under submission number K091584, sponsored by Merit Medical Systems, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2009-10-09.

Classification & Regulation

This clearance is catalogued under FDA product code DRE and 21 CFR 870.1310, within the Cardiovascular review panel as a Class II device.