Medical Device Manufacturer · US , Atlanta , GA

Cardiomems, Inc. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 2005

5

Total

4

Cleared

1

Denied

Cardiomems, Inc. has 4 FDA 510(k) cleared medical devices. Based in Atlanta, US.

Historical record: 4 cleared submissions from 2005 to 2008. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Cardiomems, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Cardiomems, Inc.

5 devices

1-5 of 5

Cleared Aug 19, 2008

CARDIOMEMS ENDOSURE S2 PRESSURE SENSOR WITH DELIVERY SYSTEM, MODEL S2-2080

Cardiovascular · 15d

Cleared Apr 05, 2007

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

Cardiovascular · 24d

Cleared Mar 15, 2007

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

Cardiovascular · 28d

Cleared Oct 12, 2006

CARDIOMEMS ENDOSURE PRESSURE SENSOR WITH DELIVERY SYSTEM, MODEL ADS-1001 AND...

Cardiovascular · 181d

Not Cleared Oct 28, 2005

CARDIOMEMS ENDOSENSOR WITH DELIVERY SYSTEM AND ENDOSENSOR ELECTRONICS SYSTEM

DEN050006 · NQH

Cardiovascular · 80d