# K810460: Burron Percutaneous Inducer Set

- Pathway: 510(k) (Traditional)
- Applicant: Burron Medical Products, Inc.
- Decided: Mar 11, 1981 after 19 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
No predicates in its family tree.
28 later devices descend from it; 2 cite it directly.
0 of 29 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021094: Introcan Safety IV Catheter (2002), 26 descendants of its own
- K111236: Introcan Safety (R) 3 Closed IV Catheter 18GA X 1-3/4 (45MM) and 18GA X 1-1/4 (32MM) / 20GA X 1-1/4 (32MM) / 20GA X 1 (2011), 15 descendants of its own
- K163358: Introcan Safety 3 Closed IV Catheter (2017), 9 descendants of its own
- K182870: Introcan Safety 3 Closed IV Catheter (2019), 8 descendants of its own
- K030135: Safety Introducer Needle (2003), 7 descendants of its own

Source page: https://510kreport.com/device/K810460
Methodology: https://510kreport.com/methodology