# Fluidsense Corp.

- Location (FDA's records): Newburyport, MA
- FDA decisions: 2 (1998–2000): 2 510(k) clearances
- Product codes: FRN (2)
- 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
- Imed Corp.: 1 (https://510kreport.com/company/imed)
- Abbott Laboratories: 1 (https://510kreport.com/company/abbott-laboratories)
- Solopak Medical Products, Inc.: 1 (https://510kreport.com/company/solopak-medical-products)

## Recent decisions
- K003582: Fluidsense Fluid Delivery System Model FS-01 (Dec 5, 2000)
- K982170: Fluidsense Fluid Delivery System (Nov 30, 1998)

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