Stethographics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Stethographics, Inc. makes
Stethographics, Inc. manufactures diagnostic systems for analyzing lung and heart sounds, including the STG Multichannel Lung Sound Analysis System and the Heart STG System with associated software. These devices capture and process acoustic data to assist in respiratory and cardiovascular assessments.
The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The portfolio is regulated in the United States, where the manufacturer is based.
Catalogue
Stg Multichannel Lung Sound Analysis System Ref K012387
Regimes: 510(k) Registry: 510(k)Heart Stg System And Software Ref K052283
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Stethographics, Inc. have in the registry?
The registry currently lists 2 devices for Stethographics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Stethographics, Inc.'s devices?
Among its 2 most recently registered devices, Stethographics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Stethographics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Stethographics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Stethographics, Inc. in the registry?
The most recently registered devices listed for Stethographics, Inc. include STG MULTICHANNEL LUNG SOUND ANALYSIS SYSTEM and HEART STG SYSTEM AND SOFTWARE.