# K071665: Scoutpro Slitter Tool Advanced, Model 356 552

- Pathway: 510(k) (Special)
- Applicant: Biotronik, Inc.
- Decided: Jul 18, 2007 after 30 days
- Product code: DQY (Catheter, Percutaneous)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K893658 (1989). 11 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 15 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K060807: Scoutpro 7F Coronary Sinus Lead Delivery System, Biotronik, Inc. (2006) Summary page 1.

## Most influential descendants
- K072329: Scoutpro 8F, 7F and Slitter Tool Advanced (2008), 2 descendants of its own
- K093303: Scoutpro 7F Long Catheters (2009), 0 descendants of its own
- K080988: Scoutpro CS Lead Introducer System (2008), 0 descendants of its own

## Indications for use
The ScoutPro Slitter Tool Advanced is used in conjunction with the ScoutPro CS Lead Introducer System to facilitate lead implantation in the left of the heart via the coronary sinus.

Source page: https://510kreport.com/device/K071665
Methodology: https://510kreport.com/methodology