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CARDIOMEMS ENDOSURE WIRELESS AAA PRESSURE MEASUREMENT SYSTEM, MODEL ADS-1001

K070448 Class II Abbreviated
Decision Date
2007-03-15
Sponsor / Applicant
Cardiomems, Inc.

Technical Specification

510(k) Submission ID K070448
Product Code NQH
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2855
Decision Date 2007-03-15
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARDIOMEMS ENDOSURE WIRELESS AAA PRESSURE MEASUREMENT SYSTEM, MODEL ADS-1001 received FDA 510(k) clearance under submission number K070448, sponsored by Cardiomems, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2007-03-15.

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.