# DEN050006: Cardiomems Endosensor with Delivery System and Endosensor Electronics System

- Pathway: De Novo (Post-NSE)
- Applicant: Cardiomems, Inc.
- Decided: Oct 28, 2005 after 80 days
- Product code: NQH (Sensor, Pressure, Aneurysm, Implantable)
- Device class: 2
- Regulation: 21 CFR 870.2855
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. De Novo decisions do not claim a predicate device.

Source page: https://510kreport.com/device/DEN050006
Methodology: https://510kreport.com/methodology