# First Source, Inc.

- Location (FDA's records): Rochester, NY
- FDA decisions: 3 (2021–2024): 3 510(k) clearances
- Product codes: IZL (2), MQB (1)
- 510(k) review time since 2016: median 96 days, against 89 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Minxray, Inc.: 2 (https://510kreport.com/company/minxray)
- Livermoretech, Inc.: 1 (https://510kreport.com/company/livermoretech)

## Recent decisions
- K240009: iQFlex Pro (Jul 3, 2024)
- K221081: iQFlex M Mobile X-ray System, iQFlex MD Mobile X-ray System (Jun 13, 2022)
- K203703: I-Q View (Mar 24, 2021)

Source page: https://510kreport.com/company/first-source