Electromics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Electromics, Inc. makes
Electromics, Inc. manufactures cardiovascular disposable products, including filtered and non-filtered cardiotomy reservoirs used in surgical procedures to manage blood during cardiac operations.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Cardiotomy Reservoir-Filtered & Non Ref K830727
Regimes: 510(k) Registry: 510(k)Cardiovascular Disposable Products Ref K830728
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Electromics, Inc. have in the registry?
The registry currently lists 2 devices for Electromics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Electromics, Inc.'s devices?
Among its 2 most recently registered devices, Electromics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Electromics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Electromics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Electromics, Inc. in the registry?
The most recently registered devices listed for Electromics, Inc. include CARDIOTOMY RESERVOIR-FILTERED & NON and CARDIOVASCULAR DISPOSABLE PRODUCTS.