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CONTRAST CONSERVATION SYSTEM

K131478 Class II Traditional
Decision Date
2013-08-15
Sponsor / Applicant
Osprey Medical, Inc.

Technical Specification

510(k) Submission ID K131478
Product Code DXT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1650
Decision Date 2013-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONTRAST CONSERVATION SYSTEM received FDA 510(k) clearance under submission number K131478, sponsored by Osprey Medical, 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 2013-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code DXT and 21 CFR 870.1650, within the Cardiovascular review panel as a Class II device.