Cardio-Med-Associates, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cardio-Med-Associates, Inc. makes
Cardio-Med-Associates, Inc. manufactures surgical device packs including the CARDIO-PAK LAPAROTOMY PACK and CARDIO-PAK BASIC PUMP PACK.
The company's products are Class II devices listed in the FDA 510(k) registry, and Cardio-Med-Associates, Inc. is based in the US.
Catalogue
Cardio-Pak Laparotomy Pack Ref K923233
Regimes: 510(k) Registry: 510(k)Cardio-Pak Basic Pump Pack Ref K923231
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cardio-Med-Associates, Inc. have in the registry?
The registry currently lists 2 devices for Cardio-Med-Associates, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cardio-Med-Associates, Inc.'s devices?
Among its 2 most recently registered devices, Cardio-Med-Associates, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cardio-Med-Associates, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cardio-Med-Associates, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cardio-Med-Associates, Inc. in the registry?
The most recently registered devices listed for Cardio-Med-Associates, Inc. include CARDIO-PAK LAPAROTOMY PACK and CARDIO-PAK BASIC PUMP PACK.