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TRILLIUM BIO DISPOSABLE BLOOD FLOW PROBE (MODELS DP38T & FP38P)

K012747 Class II Special
Decision Date
2001-09-14
Sponsor / Applicant
Medtronic Perfusion Systems

Technical Specification

510(k) Submission ID K012747
Product Code DPT
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2120
Decision Date 2001-09-14
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRILLIUM BIO DISPOSABLE BLOOD FLOW PROBE (MODELS DP38T & FP38P) received FDA 510(k) clearance under submission number K012747, sponsored by Medtronic Perfusion Systems. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-09-14.

Classification & Regulation

This clearance is catalogued under FDA product code DPT and 21 CFR 870.2120, within the Cardiovascular review panel as a Class II device.