meddevicedb.com FDA Device Reference

V1 MULTI-PORT CONNECTOR, MODEL PAD V1-MPC

K062577 Class II Traditional
Decision Date
2006-12-15
Sponsor / Applicant
Tz Medical, Inc.

Technical Specification

510(k) Submission ID K062577
Product Code DSA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2900
Decision Date 2006-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

V1 MULTI-PORT CONNECTOR, MODEL PAD V1-MPC received FDA 510(k) clearance under submission number K062577, sponsored by Tz Medical, 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 2006-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code DSA and 21 CFR 870.2900, within the Cardiovascular review panel as a Class II device.