Output, Inc.
United StatesFDA 510(k) applicant, unverified
- Devices
- 5
What Output, Inc. makes
Output, Inc. manufactures digital display modules, including models 611 and 401, designed for medical and industrial applications. The company also produces nerve stimulators, such as the peripheral nerve stimulator and the model FB-800 nerve stimulator, as well as digital printers for medical use.
The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. These devices are listed in the FDA’s 510(k) registry, and the company is based in the United States.
Catalogue
Output Digital Display Module, Mod. 611 Ref K800360
510(k) 510(k)Nerve Stimulator, Molel No. Fb-800 Ref K770987
510(k) 510(k)Peripheral Nerve Stimulator Ref K760614
510(k) 510(k)Printer, Digital Ref K781115
510(k) 510(k)Output Digital Display Module, Model 401 Ref K780356
510(k) 510(k)
Frequently asked questions
How many devices does Output, Inc. have in the registry?
The registry currently lists 5 devices for Output, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Output, Inc.'s devices?
Among its 5 most recently registered devices, Output, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Output, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Output, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Output, Inc. in the registry?
The most recently registered devices listed for Output, Inc. include OUTPUT DIGITAL DISPLAY MODULE, MOD. 611, NERVE STIMULATOR, MOLEL NO. FB-800, PERIPHERAL NERVE STIMULATOR and PRINTER, DIGITAL.