meddevicedb.com FDA Device Reference

CARDIOMEMS ENDOSURE S2 14F WIRELESS AAA PRESSURE MEASUREMENT SYSTEM, MODEL# S2-2080

K070680 Class II Special
Decision Date
2007-04-05
Sponsor / Applicant
Cardiomems, Inc.

Technical Specification

510(k) Submission ID K070680
Product Code NQH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2855
Decision Date 2007-04-05
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARDIOMEMS ENDOSURE S2 14F WIRELESS AAA PRESSURE MEASUREMENT SYSTEM, MODEL# S2-2080 received FDA 510(k) clearance under submission number K070680, sponsored by Cardiomems, 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 2007-04-05.

Classification & Regulation

This clearance is catalogued under FDA product code NQH and 21 CFR 870.2855, within the Cardiovascular review panel as a Class II device.