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STOCKERT CENTRIFUGAL PUMP (SCP PLUS) (COMPLETE) OR (FOR S5/C5 SYSTEMS)

K103468 Class II Traditional
Decision Date
2011-01-20
Sponsor / Applicant
Sorin Group Deutschland GmbH

Technical Specification

510(k) Submission ID K103468
Product Code DWA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4380
Decision Date 2011-01-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STOCKERT CENTRIFUGAL PUMP (SCP PLUS) (COMPLETE) OR (FOR S5/C5 SYSTEMS) received FDA 510(k) clearance under submission number K103468, sponsored by Sorin Group Deutschland GmbH. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2011-01-20.

Classification & Regulation

This clearance is catalogued under FDA product code DWA and 21 CFR 870.4380, within the Cardiovascular review panel as a Class II device.