# The R Group

- Location (FDA's records): Gainesvilles, FL
- FDA decisions: 4 (1991–1991): 4 510(k) clearances
- Product codes: DQO (1), FOZ (1), DXT (1), DRE (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
- K905415: Braided High Pressure Catheter Connector (Aug 12, 1991)
- K912076: Poly Braided Pigtail/Perc Card Cath W/Var Tip Conf (Jul 30, 1991)
- K911549: Injector Fill Tube (Jul 18, 1991)
- K905416: Vessel Dilator (Mar 25, 1991)

Source page: https://510kreport.com/company/r-group