Naltiac Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Naltiac Medical, Inc. makes
Naltiac Medical, Inc. manufactures cannulas for cardioplegia delivery, including antegrade and retrograde models with integrated retrograde cardioplegia cannula-suction systems (RCCS), as well as perfusion sets designed for vein graft procedures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company’s products are listed in the FDA’s 510(k) database, reflecting their compliance with US medical device regulations.
Catalogue
Nmi Antegrad Cardioplegia Cannula Ref K961180
Regimes: 510(k) Registry: 510(k)Nmi Retrograde Cardioplegia Cannula-Rccs Ref K961717
Regimes: 510(k) Registry: 510(k)Nmi Vein Graft Perfusion Set Ref K961181
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Naltiac Medical, Inc. have in the registry?
The registry currently lists 3 devices for Naltiac Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Naltiac Medical, Inc.'s devices?
Among its 3 most recently registered devices, Naltiac Medical, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Naltiac Medical, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Naltiac Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Naltiac Medical, Inc. in the registry?
The most recently registered devices listed for Naltiac Medical, Inc. include NMI ANTEGRAD CARDIOPLEGIA CANNULA, NMI RETROGRADE CARDIOPLEGIA CANNULA-RCCS and NMI VEIN GRAFT PERFUSION SET.