# Xablecath, Inc.

- Location (FDA's records): Salt Lake City, UT
- FDA decisions: 3 (2017–2019): 3 510(k) clearances
- Product codes: DQY (2), PDU (1)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 1 (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
- Bridgepoint Medical: 1 (https://510kreport.com/company/bridgepoint-medical)
- Qxmedical, LLC: 1 (https://510kreport.com/company/qxmedical)

## Its most-cited devices
- K170041: XableCath Support Catheter (2017), cited by 1

## Recent decisions
- K183357: XableCath Crossing Catheter (Jan 21, 2019)
- K180986: XableCath Support Catheter Product Family (May 15, 2018)
- K170041: XableCath Support Catheter (Sep 7, 2017)

Source page: https://510kreport.com/company/xablecath