# K020680: Prowler Select 10 and 14 Infusion Catheters with and Without Pre-Shaped Tips

- Pathway: 510(k) (Special)
- Applicant: Cordis Neurovascular, Inc.
- Decided: Mar 27, 2002 after 23 days
- Product code: KRA (Catheter, Continuous Flush)
- Device class: 2
- Regulation: 21 CFR 870.1210
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K945904 (1995). 6 ancestors in all.
35 later devices descend from it; 2 cite it directly.
0 of 42 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K965181: Ces Infusion Catheter, Cordis Neurovascular, Inc. (1997) Summary page 2.
- K972518: Transit/Rapidtransit/Speedster/Prowler Infusion Catheter, Cordis Neurovascular, Inc. (1997) Summary page 2.
- K993266: Prowler Plus Infusion Catheter, Cordis Neurovascular, Inc. (1999) Summary page 2.
- K003925: Prowler Infusion Catheters with Pre-Shaped Tips, Cordis Neurovascular, Inc. (2001) Summary page 2.

## Most influential descendants
- K041123: Rinspiration System,Rinspiration System Short Tip, Models FG01477/FG01703 (2004), 17 descendants of its own
- K050130: Kerberos Proximal Solutions Rispiration System (2005), 16 descendants of its own
- K021591: Prowler Select (10, 14, and Plus) Infusion Catheters with and Without Pre-Shaped Tips (2002), 16 descendants of its own
- K062275: Rinspiration Catheter System, Models 50135, 550135, P7065, P70135 (2006), 9 descendants of its own
- K151638: Phenom 17 Catheter, Phenom 21 Catheter, Phenom 27 Catheter, Phenom Plus Catheter (2015), 6 descendants of its own

## Indications for use
The PROWLER® SELECT™ Infusion Catheters are intended to be used as a mechanism for the infusion of various diagnostic, embolic, and therapeutic agents into the vascular systems (Neuro, Peripheral, Coronary), for Guidewire Exchange/Support, and for superselective angiography of the peripheral and coronary vasculatures.

Source page: https://510kreport.com/device/K020680
Methodology: https://510kreport.com/methodology