Darox Corp.
United StatesFDA applicant, unverified
- Devices
- 2
What Darox Corp. makes
Darox Corp. manufactures external defibrillator pads (Model 480) and adaptor cables (Model 196) designed for use with automated external defibrillators (AEDs). These components facilitate electrode attachment and signal transmission during cardiac resuscitation procedures.
The company’s products are classified as Class II devices under FDA regulations and are listed via 510(k) clearance. The devices are intended for use in the United States.
Catalogue
R2 Pace Pad, Model 480 Ref K895729
Regimes: 510(k) Registry: 510(k)R2 Pace Adaptor Cable, Model 196 Ref K895728
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Darox Corp. have in the registry?
The registry currently lists 2 devices for Darox Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Darox Corp.'s devices?
Among its 2 most recently registered devices, Darox Corp. has devices listed in FDA 510(k) (2 devices).
What risk classes do Darox Corp.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Darox Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Darox Corp. in the registry?
The most recently registered devices listed for Darox Corp. include R2 PACE PAD, MODEL 480 and R2 PACE ADAPTOR CABLE, MODEL 196.