# Summit Medical Products, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 4 (2011–2017): 4 510(k) clearances
- Product codes: BSO (2), MEA (1), LJS (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 2 (0 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
- I-Flow Corp.: 2 (https://510kreport.com/company/i-flow)
- Sorenson Medical, Inc.: 1 (https://510kreport.com/company/sorenson-medical)

## Firms that cite its devices most
- Epimed International, Inc.: 1 (https://510kreport.com/company/epimed-international)
- B.Braun Medical, Inc.: 1 (https://510kreport.com/company/b-braun-medical)

## Its most-cited devices
- K102460: Ambit Introducer, Ambit Needle, Ambit Sheath (2011), cited by 2

## Recent decisions
- K162165: ambIT PCA*PIB, ambIT PIB, ambIT PIB*PCA, ambIT PIEB, and ambIT Programmable Intermittent Pump (Aug 29, 2017)
- K113043: Direct Antibiotic Infusion Kit (Dec 20, 2011)
- K110814: Ambit Tunneler (Apr 8, 2011)
- K102460: Ambit Introducer, Ambit Needle, Ambit Sheath (Jan 13, 2011)

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