Cook Pacemaker Corp.
United StatesFDA applicant, unverified
- Devices
- 35
What Cook Pacemaker Corp. makes
The company manufactures cardiac pacing devices, including unipolar and bipolar endocardial leads for implantation, programmable pulse generators for pacing signals, and handheld transceivers for programming and monitoring these systems. Products also include specialized tools like the Needle’s Eye Snare for procedural assistance in cardiac interventions.
These devices are regulated under FDA classifications, with leads and pulse generators falling under Class II and III, respectively. Authorisation records include 510(k) clearances and Premarket Approval Applications (PMA). The company is based in the United States.
Catalogue
Search and filter all 35 devicesFrequently asked questions
How many devices does Cook Pacemaker Corp. have in the registry?
The registry currently lists 35 devices for Cook Pacemaker Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cook Pacemaker Corp.'s devices?
Among its 35 most recently registered devices, Cook Pacemaker Corp. has devices listed in FDA 510(k) (34 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cook Pacemaker Corp.'s devices fall under?
Among its 35 most recently registered devices, the classes recorded for Cook Pacemaker Corp.'s devices are Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Cook Pacemaker Corp. in the registry?
The most recently registered devices listed for Cook Pacemaker Corp. include NEEDLE'S EYE SNARE, MODEL P IN-LINE BIPOLAR ENDOCARDIAL TINED LEAD, COOK PACEMAKER CORP. 327T, SERIES R UNIPOLAR CARDI and MODEL F UNIPOLAR ENDOCARDIAL LEAD-.