Anetec, Inc.
CanadaFDA applicant, unverified
- Devices
- 2
What Anetec, Inc. makes
Anetec, Inc. manufactures disposable medical devices for anesthesia applications, including transparent anesthesia filters and thermoplastic anesthesia breathing circuits designed for single-use in clinical settings.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These items are listed in the FDA’s 510(k) clearance registry and are intended for use in the United States.
Catalogue
Transparent Anesthesia Filter Ref K944189
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anetec, Inc. have in the registry?
The registry currently lists 2 devices for Anetec, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anetec, Inc.'s devices?
Among its 2 most recently registered devices, Anetec, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anetec, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anetec, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anetec, Inc. in the registry?
The most recently registered devices listed for Anetec, Inc. include TRANSPARENT ANESTHESIA FILTER and DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS.