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MODIFIED MODEL SC4000(F) CARDIOTOMY RESERVOIR

K855049 Class II Traditional
Decision Date
1986-02-26
Sponsor / Applicant
Scimed Life Systems, Inc.

Technical Specification

510(k) Submission ID K855049
Product Code DTP
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4230
Decision Date 1986-02-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFIED MODEL SC4000(F) CARDIOTOMY RESERVOIR received FDA 510(k) clearance under submission number K855049, sponsored by Scimed Life Systems, 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 1986-02-26.

Classification & Regulation

This clearance is catalogued under FDA product code DTP and 21 CFR 870.4230, within the Cardiovascular review panel as a Class II device.