Cone Instruments, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Cone Instruments, Inc. makes
Cone Instruments, Inc. manufactures real-time ultrasound scanners, including the COMBISON 310A and COMBISON R 320A, as well as diagnostic software like ECHO-COM for MS-Windows and medical enema tubes.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.
Catalogue
Combison(R) 310A Real Time Ultrasound Scanner Ref K873159
Regimes: 510(k) Registry: 510(k)Echo-Com For Ms-Windows Version 2.0 Ref K960665
Regimes: 510(k) Registry: 510(k)Enema Tube Ref K832501
Regimes: 510(k) Registry: 510(k)Combison R 320A Ref K861376
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cone Instruments, Inc. have in the registry?
The registry currently lists 4 devices for Cone Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cone Instruments, Inc.'s devices?
Among its 4 most recently registered devices, Cone Instruments, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Cone Instruments, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Cone Instruments, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cone Instruments, Inc. in the registry?
The most recently registered devices listed for Cone Instruments, Inc. include COMBISON(R) 310A REAL TIME ULTRASOUND SCANNER, ECHO-COM FOR MS-WINDOWS VERSION 2.0, ENEMA TUBE and COMBISON R 320A.