# Intuit Medical Products, LLC

- Location (FDA's records): Sugar Hill, GA
- FDA decisions: 3 (2015–2020): 3 510(k) clearances
- Product codes: LRC (2), KTI (1)
- Predicates its devices cite: 4 (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
- Acclarent, Inc.: 4 (https://510kreport.com/company/acclarent)

## Recent decisions
- K181546: Dillard Nasal Balloon Catheter (Jan 3, 2020)
- K153484: Dillard Airway Dilatation System (Jul 27, 2016)
- K143738: DSS Sinusplasty Balloon Catheter (Aug 27, 2015)

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