# Barosense, Inc.

- Location (FDA's records): Redwood City, CA
- FDA decisions: 5 (2009–2012): 5 510(k) clearances
- Product codes: OCW (3), FED (2)
- Predicates its devices cite: 9 (3 its own); citations of its devices by later devices: 3 (3 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
- United States Endoscopy Group, Inc.: 1 (https://510kreport.com/company/united-states-endoscopy-group)
- Surgical, Inc.: 1 (https://510kreport.com/company/surgical)
- C.R. Bard, Inc.: 1 (https://510kreport.com/company/cr-bard)
- Endogastric Solutions, Inc.: 1 (https://510kreport.com/company/endogastric-solutions)
- Lsi Solutions: 1 (https://510kreport.com/company/lsi-solutions)
- Ndo Surgical, Inc.: 1 (https://510kreport.com/company/ndo-surgical)

## Its most-cited devices
- K082589: Barosense Endogastric Tube (Egt), Model F0034 (2009), cited by 1
- K082044: Ace Stapler, Model F0031 (2010), cited by 1
- K110829: Ace Stapler and Cartridge (2011), cited by 1

## Recent decisions
- K120126: Barosense Endogastric Tube and Introducer Bougie (Sep 10, 2012)
- K120147: Ace Stapler and Cartridge (Feb 17, 2012)
- K110829: Ace Stapler and Cartridge (Jun 3, 2011)
- K082044: Ace Stapler, Model F0031 (May 11, 2010)
- K082589: Barosense Endogastric Tube (Egt), Model F0034 (May 22, 2009)

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