Heyer America, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Heyer America, Inc. makes
Heyer America, Inc. manufactures medical devices including the Narkomat Model 2000 for anesthesia delivery, the Anodyne CC for pain management, the Minitrop Aerosol Unit for respiratory therapy, and the Modular system for patient monitoring and infusion therapy.
These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company is based in the United States.
Catalogue
Narkomat, Model 2000 Ref K000995
Regimes: 510(k) Registry: 510(k)Anodyne Cc Ref K963481
Regimes: 510(k) Registry: 510(k)Minitrop Aerosol Unit Ref K912566
Regimes: 510(k) Registry: 510(k)Modular Ref K001988
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Heyer America, Inc. have in the registry?
The registry currently lists 4 devices for Heyer America, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Heyer America, Inc.'s devices?
Among its 4 most recently registered devices, Heyer America, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Heyer America, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Heyer America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Heyer America, Inc. in the registry?
The most recently registered devices listed for Heyer America, Inc. include NARKOMAT, MODEL 2000, ANODYNE CC, MINITROP AEROSOL UNIT and MODULAR.