Angemed, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Angemed, Inc. makes
Angemed, Inc. manufactures medical leads, including the ANGEMED 5000 Lead Adapter for pacemaker or implantable cardioverter-defibrillator (ICD) systems, and the ANGEMED Model 4000 QC Bipolar Temporary Pacing Lead for temporary cardiac stimulation.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Angemed 5000 Lead Adapter Ref K924390
Regimes: 510(k) Registry: 510(k)Angemed Model 4000 Qc Bipolar Temp Pacing Lead Ref K924388
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angemed, Inc. have in the registry?
The registry currently lists 2 devices for Angemed, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angemed, Inc.'s devices?
Among its 2 most recently registered devices, Angemed, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Angemed, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Angemed, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angemed, Inc. in the registry?
The most recently registered devices listed for Angemed, Inc. include ANGEMED 5000 LEAD ADAPTER and ANGEMED MODEL 4000 QC BIPOLAR TEMP PACING LEAD.