# Interrad Medical, Inc.

- Location (FDA's records): Plymouth, MN
- FDA decisions: 7 (2008–2021): 7 510(k) clearances
- Product codes: OKC (5), KMK (1), LJS (1)
- Predicates its devices cite: 13 (7 its own); citations of its devices by later devices: 7 (7 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
- Bard Access Systems, Inc.: 2 (https://510kreport.com/company/bard-access-systems)
- Venetec, Inc.: 2 (https://510kreport.com/company/venetec)
- AngioDynamics, Inc.: 1 (https://510kreport.com/company/angiodynamics)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)

## Its most-cited devices
- K082047: Securacath Catheter, Model SPK01 (2008), cited by 2
- K120935: Securacath (2012), cited by 1
- K083081: Modification to Securacath, Model: SPK01 (2009), cited by 1
- K180994: SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F (2019), cited by 1
- K092306: Securacath Universal (2010), cited by 1
- K180769: SecurAcath (2018), cited by 1

## Recent decisions
- K210629: SecurAcath (Apr 12, 2021)
- K180994: SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcath 8F (Jul 9, 2019)
- K180769: SecurAcath (Jun 26, 2018)
- K120935: Securacath (Apr 27, 2012)
- K092306: Securacath Universal (Jul 9, 2010)
- K083081: Modification to Securacath, Model: SPK01 (Mar 4, 2009)
- K082047: Securacath Catheter, Model SPK01 (Sep 30, 2008)

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