Verite Scientific, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Verite Scientific, Inc. makes
Verite Scientific, Inc. manufactures electrocardiogram (ECG) lead systems, including the VERI/CTGS Model 850 for continuous telemetry and the VERI/TRODES for disposable ECG electrodes. These products are designed for patient monitoring in clinical and ambulatory settings, facilitating accurate cardiac signal acquisition.
The company’s portfolio is regulated under FDA Class II devices, with products listed via the 510(k) clearance pathway. The devices are intended for use in the United States, where compliance with FDA regulations applies. No additional international registries are referenced.
Catalogue
Veri/Ctgs Model 850 Ref K771122
Regimes: 510(k) Registry: 510(k)Veri/Trodes Ref K770323
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Verite Scientific, Inc. have in the registry?
The registry currently lists 2 devices for Verite Scientific, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Verite Scientific, Inc.'s devices?
Among its 2 most recently registered devices, Verite Scientific, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Verite Scientific, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Verite Scientific, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Verite Scientific, Inc. in the registry?
The most recently registered devices listed for Verite Scientific, Inc. include VERI/CTGS MODEL 850 and VERI/TRODES.