Procare C/O Wiley, Rein & Fielding
Country not established
- Devices
- 1
What Procare C/O Wiley, Rein & Fielding makes
The company produces educational kits designed to provide information about gender identity, including separate materials for female and male perspectives. These kits are intended for use in clinical or educational settings to support discussions related to gender diversity and identity.
The portfolio is regulated under Class II (U) devices in the United States and is listed in the FDA’s 510(k) clearance registry. The company operates from the United States.
Catalogue
Gender Choice Information Kit, Female And Male Ref K870999
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Procare C/O Wiley, Rein & Fielding have in the registry?
The registry currently lists 1 device for Procare C/O Wiley, Rein & Fielding. Devices recorded under merged duplicate company entries are counted once.
Which registries list Procare C/O Wiley, Rein & Fielding's devices?
Among its 1 most recently registered device, Procare C/O Wiley, Rein & Fielding has devices listed in FDA 510(k) (1 device).
What are the newest devices from Procare C/O Wiley, Rein & Fielding in the registry?
The most recently registered devices listed for Procare C/O Wiley, Rein & Fielding include GENDER CHOICE INFORMATION KIT, FEMALE AND MALE.