Disco, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Disco, Inc. makes
Disco, Inc. manufactures a femoral artery pressure pad or disk, designed for vascular access or monitoring, and the QuickLamp System, a handheld device likely used for vascular illumination or procedural guidance.
The company’s portfolio is regulated under FDA Class II devices and includes products listed via the 510(k) clearance pathway. Disco, Inc. is based in the United States.
Catalogue
Femoral Artery Pressure Pad/Disk Ref K914149
Regimes: 510(k) Registry: 510(k)Quicklamp System Ref K923085
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Disco, Inc. have in the registry?
The registry currently lists 2 devices for Disco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Disco, Inc.'s devices?
Among its 2 most recently registered devices, Disco, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Disco, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Disco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Disco, Inc. in the registry?
The most recently registered devices listed for Disco, Inc. include FEMORAL ARTERY PRESSURE PAD/DISK and QUICKLAMP SYSTEM.