# K014109: IN-Time Retrieval Device

- Pathway: 510(k) (Traditional)
- Applicant: Boston Scientific, Target
- Decided: Mar 12, 2002 after 88 days
- Product code: MMX (Device, Percutaneous Retrieval)
- Device class: 2
- Regulation: 21 CFR 870.5150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K914067 (1991). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K914067: Retrieval Device, Target Therapeutics (1991) Summary page 1.

## Most influential descendants
- K093977: Alligator-HD Retrieval Device (Ard-HD), Model FA-88840-XX (2010), 0 descendants of its own
- K091563: Recruit Microcatheter (2009), 0 descendants of its own

## Indications for use
The In-Time™ Retrieval Device is designed for use with a guiding catheter for the retrieval of intravascular foreign objects such as coils, balloons, portions of catheters and / or loop wires misplaced during interventional radiologic procedures in peripheral, neuro and cardiovasculature.

Source page: https://510kreport.com/device/K014109
Methodology: https://510kreport.com/methodology