# Med2000 S.R.L.

- Location (FDA's records): Great Neck, NY
- FDA decisions: 3 (2004–2004): 3 510(k) clearances
- Product codes: CAF (2), BTI (1)
- Predicates its devices cite: 6 (2 its own); citations of its devices by later devices: 3 (2 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
- Salter Labs: 2 (https://510kreport.com/company/salter-labs)
- Respironics Healthscan, Inc.: 1 (https://510kreport.com/company/respironics-healthscan)
- Galemed Corp.: 1 (https://510kreport.com/company/galemed)

## Firms that cite its devices most
- K-Jump Health Co., Ltd.: 1 (https://510kreport.com/company/k-jump-health)

## Its most-cited devices
- K031908: MED2000 Spa Nebulizer Compressors, Models P1 and P2, with Nebulizer, and MED2000 Spa Nebulizer, Model A1/C (Andyflow) (2004), cited by 3

## Recent decisions
- K041974: MED2000 Nebulizer Compressor, Models P3, P4, P5 with Nebulizer (Aug 24, 2004)
- K041327: MED2000 Spa Nebulizer Andyflow, Model A1/C with Accessories (Jul 20, 2004)
- K031908: MED2000 Spa Nebulizer Compressors, Models P1 and P2, with Nebulizer, and MED2000 Spa Nebulizer, Model A1/C (Andyflow) (Jan 14, 2004)

Source page: https://510kreport.com/company/med2000