Nutec, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Nutec, Inc. makes
Nutec, Inc. manufactures respiratory and airway management devices, including a double tracheal swivel connector for secure tube attachment, a hyperinflation bag system for manual ventilation, and a hand-held nebulizer for aerosolized medication delivery.
The company’s portfolio includes Class I and Class II devices, with products authorised via the FDA’s 510(k) pathway. These devices are listed under US regulatory requirements, and the company operates from the United States.
Catalogue
Double Trach Swivel Connector Ref K935821
Regimes: 510(k) Registry: 510(k)Hyperinflation Bag System Ref K940255
Regimes: 510(k) Registry: 510(k)Hand-Held Nebulizer Ref K940257
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nutec, Inc. have in the registry?
The registry currently lists 3 devices for Nutec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nutec, Inc.'s devices?
Among its 3 most recently registered devices, Nutec, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Nutec, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Nutec, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nutec, Inc. in the registry?
The most recently registered devices listed for Nutec, Inc. include DOUBLE TRACH SWIVEL CONNECTOR, HYPERINFLATION BAG SYSTEM and HAND-HELD NEBULIZER.