# K801941: Burron Microcath Intra. Cath. Placementt

- Pathway: 510(k) (Traditional)
- Applicant: Burron Medical Products, Inc.
- Decided: Aug 27, 1980 after 14 days
- Product code: FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5200
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
72 later devices descend from it; 2 cite it directly.
0 of 73 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
- K982805: Introcan Safety IV Catheter (1999), 70 descendants of its own
- K020785: Introcan Safety IV Catheter (2002), 55 descendants of its own
- K021094: Introcan Safety IV Catheter (2002), 26 descendants of its own
- K101422: The Power Wand Safety Introducer with an Extended Dwell Catheter (2011), 25 descendants of its own
- K121073: Powerglide Midline Catheter (2012), 19 descendants of its own

Source page: https://510kreport.com/device/K801941
Methodology: https://510kreport.com/methodology