# Richard-Allan Medical

- Location (FDA's records): Richland, MI
- FDA decisions: 8 (1991–1994): 8 510(k) clearances
- Product codes: GEI (2), GEF (1), KKX (1), HBT (1), HIF (1), GAG (1), FSM (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
- K942207: Reflex Ins Insufflation Needle (May 27, 1994)
- K935105: Reflex Esp with Finger Switches (Feb 22, 1994)
- K933508: Reflex SDD Surgical Stapler (Nov 23, 1993)
- K933901: Reflex (R) Ehs (Endoscopic Hernia Stapler) (Nov 19, 1993)
- K924881: Reflex (R) Esp (Jul 23, 1993)
- K924929: Reflex (R) Eca (Jul 21, 1993)
- K905701: Richard-Allan Sheet Clip (Feb 19, 1991)
- K905682: Richard-Allan Clamp Covers (Feb 19, 1991)

Source page: https://510kreport.com/company/richard-allan-medical