# Mercator Medsystems, Inc.

- Location (FDA's records): Emeryville, CA
- FDA decisions: 5 (2006–2021): 5 510(k) clearances
- Product codes: KRA (4), EOQ (1)
- 510(k) review time since 2016: median 130 days, against 122 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 9 (4 its own); citations of its devices by later devices: 7 (4 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
- Ablative Solutions, Inc.: 1 (https://510kreport.com/company/ablative-solutions)
- Endobionics, Inc.: 1 (https://510kreport.com/company/endobionics)
- Scimed Life Systems, Inc.: 1 (https://510kreport.com/company/scimed-life-systems)
- Advanced Cardiovascular Systems, Inc.: 1 (https://510kreport.com/company/advanced-cardiovascular-systems)
- Lake Region Mfg., Inc.: 1 (https://510kreport.com/company/lake-region-mfg)

## Firms that cite its devices most
- Ablative Solutions, Inc.: 1 (https://510kreport.com/company/ablative-solutions)
- Intervene: 1 (https://510kreport.com/company/intervene)
- SmartWise Sweden AB: 1 (https://510kreport.com/company/smartwise-sweden)

## Its most-cited devices
- K161402: Bullfrog Micro-Infusion Device (2016), cited by 3
- K062752: Mercator Microsyringe II Infusion Catheter (2006), cited by 3
- K153501: Bullfrog Micro-Infusion Device (2016), cited by 1

## Recent decisions
- K210339: Bullfrog Micro-Infusion Device (Aug 2, 2021)
- K161402: Bullfrog Micro-Infusion Device (Aug 18, 2016)
- K153501: Bullfrog Micro-Infusion Device (Apr 15, 2016)
- K131401: Blowfish Transbronchial Micro-Infusion Catheter (Jul 2, 2013)
- K062752: Mercator Microsyringe II Infusion Catheter (Dec 7, 2006)

Source page: https://510kreport.com/company/mercator-medsystems