# Procare C/O Wiley, Rein & Fielding

- Location (FDA's records): Washington, DC
- FDA decisions: 1 (1987–1987): 1 510(k) clearance
- Product codes: LHD (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K870999: Gender Choice Information Kit, Female and Male (Jul 14, 1987)

Source page: https://510kreport.com/company/procare-c-o-wiley-rein-fielding