# Sedat

- Location (FDA's records): San Diego, CA
- FDA decisions: 5 (2004–2008): 5 510(k) clearances
- Names in FDA's records: Sedat (3); Sedat S.A. (2)
- Product codes: DTL (2), MAV (2), DQO (1)
- Predicates its devices cite: 5 (3 its own); citations of its devices by later devices: 8 (3 its own)
- Recalls linked to its devices: 5 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Advanced Cardiovascular Systems, Inc.: 1 (https://510kreport.com/company/advanced-cardiovascular-systems)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)

## Firms that cite its devices most
- France Chirurgae Instrumentation: 1 (https://510kreport.com/company/france-chirurgae-instrumentation)
- Merit Medical Systems, Inc.: 1 (https://510kreport.com/company/merit-medical-systems)
- Vascular Solutions, Inc.: 1 (https://510kreport.com/company/vascular-solutions)
- Oxti Corporation: 1 (https://510kreport.com/company/oxti)
- Needle Tech Products, Inc.: 1 (https://510kreport.com/company/needle-tech-products)

## Its most-cited devices
- K040498: Myshell (2004), cited by 4
- K042449: Dolphin Inflation Device (2005), cited by 2
- K082755: Sedat Flamingo (2008), cited by 2

## Recent decisions
- K082755: Sedat Flamingo (Dec 15, 2008)
- K080472: Sedat Myshell Lite (Apr 23, 2008)
- K060010: Nautiflux (Aug 4, 2006)
- K042449: Dolphin Inflation Device (Apr 18, 2005)
- K040498: Myshell (Jul 2, 2004)

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