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BIOSPHERE MEDICAL INFUSION CATHETER

K003105 Class II Traditional
Decision Date
2001-05-22
Sponsor / Applicant
Biosphere Medical

Technical Specification

510(k) Submission ID K003105
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2001-05-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOSPHERE MEDICAL INFUSION CATHETER received FDA 510(k) clearance under submission number K003105, sponsored by Biosphere Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-05-22.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.