Thinklabs, Inc.
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- Devices
- 1
What Thinklabs, Inc. makes
Thinklabs, Inc. manufactures the RHYTHM DIGITAL ELECTRONIC STETHOSCOPE, a medical device used for auscultation.
The RHYTHM DIGITAL ELECTRONIC STETHOSCOPE is classified as a Class II device and is listed in the FDA 510(k) registry. Thinklabs, Inc. is based in the US.
Catalogue
Rhythm Digital Electronic Stethoscope Ref K032230
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Thinklabs, Inc. have in the registry?
The registry currently lists 1 device for Thinklabs, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Thinklabs, Inc.'s devices?
Among its 1 most recently registered device, Thinklabs, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Thinklabs, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Thinklabs, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Thinklabs, Inc. in the registry?
The most recently registered devices listed for Thinklabs, Inc. include RHYTHM DIGITAL ELECTRONIC STETHOSCOPE.