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MISER CONTRAST MANAGEMENT SYSTEM

K083576 Class II Special
Decision Date
2008-12-23
Sponsor / Applicant
Merit Medical Systems, Inc.

Technical Specification

510(k) Submission ID K083576
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2008-12-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MISER CONTRAST MANAGEMENT SYSTEM received FDA 510(k) clearance under submission number K083576, sponsored by Merit Medical Systems, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2008-12-23.

Classification & Regulation

This clearance is catalogued under FDA product code FPA and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.