meddevicedb.com FDA Device Reference

MVR 1200 PC: SORIN MONOLYTH VENOUS RESERVOIR 1200 PC WITH PHOSPHORYLCHOLINE COATING

K033714 Class II Special
Decision Date
2003-12-11
Sponsor / Applicant
Dideco S.P.A.

Technical Specification

510(k) Submission ID K033714
Product Code DTN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4400
Decision Date 2003-12-11
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MVR 1200 PC: SORIN MONOLYTH VENOUS RESERVOIR 1200 PC WITH PHOSPHORYLCHOLINE COATING received FDA 510(k) clearance under submission number K033714, sponsored by Dideco S.P.A.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code DTN and 21 CFR 870.4400, within the Cardiovascular review panel as a Class II device.