# Regulatory & Marketing Services, Inc.

- Location (FDA's records): Palm Harbor, FL
- FDA decisions: 21 (1993–1996): 21 510(k) clearances
- Product codes: EZL (6), FGM (3), GBX (2), JDL (1), GZB (1), FMI (1), KNX (1), FRG (1), JOH (1), IQI (1), EZD (1), KNY (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
- K944673: Mri's All Silicone Foley Catheter Temperature Probe (Apr 10, 1996)
- K954752: Pediatric Europhylic Foley Catheter (Oct 30, 1995)
- K941342: Pain Doc (Oct 13, 1995)
- K941543: Dial Medical Kit (Feb 16, 1995)
- K944379: Orion's Foley Catheterization Kit with Catheter and Bag (Feb 15, 1995)
- K944378: Orion's Urethral Catheterization Kit with Catheter and Bag (Feb 15, 1995)
- K944384: Orion's Urethral Catheterization Kit Without Bag (Feb 15, 1995)
- K945874: Euromedical Poly Tracheotomy Tube (Dec 27, 1994)

Source page: https://510kreport.com/company/regulatory-marketing-services