Palpometer Systems, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Palpometer Systems, Inc. makes
Palpometer Systems, Inc. makes the Sonic Palpometer, a device used for palpation assessment.
The Sonic Palpometer is classified as a Class I medical device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Sonic Palpometer Ref K060125
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Palpometer Systems, Inc. have in the registry?
The registry currently lists 1 device for Palpometer Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Palpometer Systems, Inc.'s devices?
Among its 1 most recently registered device, Palpometer Systems, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Palpometer Systems, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Palpometer Systems, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Palpometer Systems, Inc. in the registry?
The most recently registered devices listed for Palpometer Systems, Inc. include SONIC PALPOMETER.