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EMBOCATH PLUS INFUSION MICROCATHETER, MODEL ECP-100 AND ECP-135

K062126 Class II Special
Decision Date
2006-08-09
Sponsor / Applicant
Biosphere Medical, Inc.

Technical Specification

510(k) Submission ID K062126
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2006-08-09
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMBOCATH PLUS INFUSION MICROCATHETER, MODEL ECP-100 AND ECP-135 received FDA 510(k) clearance under submission number K062126, sponsored by Biosphere Medical, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2006-08-09.

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.