# Intuity Medical, Inc.

- Location (FDA's records): Sunnyvale, CA
- FDA decisions: 3 (2016–2018): 3 510(k) clearances
- Product codes: NBW (3)
- 510(k) review time since 2016: median 237 days, against 233 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 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
- Roche Diagnostics Corp.: 1 (https://510kreport.com/company/roche-diagnostics)
- Bionostics, Inc.: 1 (https://510kreport.com/company/bionostics)
- Bayer Healthcare, LLC: 1 (https://510kreport.com/company/bayer-healthcare)

## Its most-cited devices
- K162203: POGO Automatic Blood Glucose Monitoring System (2017), cited by 1

## Recent decisions
- K181316: POGO Automatic Blood Glucose Monitoring System (Jun 14, 2018)
- K162203: POGO Automatic Blood Glucose Monitoring System (Apr 6, 2017)
- K152493: POGO Automatic Blood Glucose Monitoring System (Apr 25, 2016)

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