# Moss Medical Products

- Location (FDA's records): New York, NY
- FDA decisions: 8 (1991–2005): 8 510(k) clearances
- Product codes: KNT (7), FPD (1)
- Predicates its devices cite: 3 (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

## Firms whose devices it cites most
- Gelman Sciences, Inc.: 1 (https://510kreport.com/company/gelman-sciences)
- Rapid Diagnostic Laboratories, Inc.: 1 (https://510kreport.com/company/rapid-diagnostic-laboratories)
- Impact Instrumentation, Inc.: 1 (https://510kreport.com/company/impact-instrumentation)

## Recent decisions
- K051206: Y2K2 Enternal Tube Fluid Filter (Nov 2, 2005)
- K030413: Y2K2 Enternal Feeding Manager (May 11, 2004)
- K031492: Mossmed Dual Intermittent Aspirator (Feb 5, 2004)
- K913701: Moss - Anchor Set (Feb 14, 1992)
- K910910: Moss- Anchor Set (Jun 24, 1991)
- K910912: Moss Nasal Tube Mark IV (May 28, 1991)
- K910911: Moss P.E.G. Tray (May 3, 1991)
- K910913: Moss Gastrostomy Tube (Apr 19, 1991)

Source page: https://510kreport.com/company/moss-medical-products