New York Heart Instruments, Inc.
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- Devices
- 1
What New York Heart Instruments, Inc. makes
New York Heart Instruments, Inc. manufactures the EMI Model FFF-IA, a medical device designed for specific cardiac applications, including electrophysiological procedures.
The EMI Model FFF-IA is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Emi Model Fff-Ia Ref K952164
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does New York Heart Instruments, Inc. have in the registry?
The registry currently lists 1 device for New York Heart Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list New York Heart Instruments, Inc.'s devices?
Among its 1 most recently registered device, New York Heart Instruments, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do New York Heart Instruments, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for New York Heart Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from New York Heart Instruments, Inc. in the registry?
The most recently registered devices listed for New York Heart Instruments, Inc. include EMI MODEL FFF-IA.