# Solopak Medical Products, Inc.

- Location (FDA's records): Libertyville, IL
- FDA decisions: 4 (1996–1997): 4 510(k) clearances
- Product codes: MEB (2), FPA (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 5 (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
- I-Flow Corp.: 2 (https://510kreport.com/company/i-flow)
- Icu Medical, Inc.: 1 (https://510kreport.com/company/icu-medical)

## Firms that cite its devices most
- Filtertek, Inc.: 2 (https://510kreport.com/company/filtertek)
- Tandem Medical, Inc.: 1 (https://510kreport.com/company/tandem-medical)
- Fluidsense Corp.: 1 (https://510kreport.com/company/fluidsense)

## Its most-cited devices
- K960661: Maxcess Needle Free Connector (8200) (1996), cited by 3
- K962663: Solopak Sidekick Infusion Pump and Administation Set (1996), cited by 1
- K970800: Maxcess Needlefree - Y- Site (100713) (1997), cited by 1

## Recent decisions
- K970800: Maxcess Needlefree - Y- Site (100713) (Apr 2, 1997)
- K962663: Solopak Sidekick Infusion Pump and Administation Set (Oct 4, 1996)
- K963355: Solopak Paragon Infusor Pump and Infusion Set (Oct 4, 1996)
- K960661: Maxcess Needle Free Connector (8200) (Mar 21, 1996)

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