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SH14 HEMOCONCENTRATOR

K081313 Class II Abbreviated
Decision Date
2008-11-19
Sponsor / Applicant
Sorin Group Italia S.R.L.

Technical Specification

510(k) Submission ID K081313
Product Code KDI
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5860
Decision Date 2008-11-19
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SH14 HEMOCONCENTRATOR received FDA 510(k) clearance under submission number K081313, sponsored by Sorin Group Italia S.R.L.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2008-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code KDI and 21 CFR 876.5860, within the Gastroenterology, Urology review panel as a Class II device.