# Smiths Medical Ads, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 2 (2017–2018): 2 510(k) clearances
- Product codes: MEA (1), BTO (1)
- Predicates its devices cite: 3 (0 its own); citations of its devices by later devices: 5 (0 its own)
- Recalls linked to its devices: 9 (8 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Smiths Medical Asd, Inc.: 1 (https://510kreport.com/company/smiths-medical-asd)
- Smiths Medical MD, Inc.: 1 (https://510kreport.com/company/smiths-medical-md)
- Portex, Inc.: 1 (https://510kreport.com/company/portex)

## Firms that cite its devices most
- Smiths Medical Asd, Inc.: 1 (https://510kreport.com/company/smiths-medical-asd)
- Vitaltec Corporation: 1 (https://510kreport.com/company/vitaltec)
- Eitan Medical, Ltd.: 1 (https://510kreport.com/company/eitan-medical)
- Covidien: 1 (https://510kreport.com/company/covidien)
- Zevex, Inc.: 1 (https://510kreport.com/company/zevex)

## Its most-cited devices
- K173384: BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube (2018), cited by 3
- K170982: CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM) (2017), cited by 2

## Recent decisions
- K173384: BLUselect, non-fenestrated, BLUselect, non-fenestrated, cont, BLUselect, fenestrated, BLUselect Suctionaid, BLUpere Dilation Trachestomy Kit, without tube (Apr 10, 2018)
- K170982: CADD®- Solis Ambulatory Infusion Pump with Wireless Communication; CADD®-Solis Infusion Pump, Model 2110; PharmGuard® Administrator Medication Safety Software; CADD® Administration Sets; Wireless Communication Module (CM) (Aug 24, 2017)

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