# K932323: Percutaneous Introducer

- Pathway: 510(k) (Traditional)
- Applicant: Medamicus, Inc.
- Decided: Nov 9, 1993 after 182 days
- Product code: DYB (Introducer, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
67 later devices descend from it; 2 cite it directly.
0 of 68 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K990705: Medamicus Coaxial Introducer Kit, 10330-XXX, Boston Scientific Coaxial Dilator Set (1999), 48 descendants of its own
- K071574: Stiffer Coaxial Micro-Introducer Kit (2007), 45 descendants of its own
- K090372: The Wand Microaccess Safety Introducer (2009), 32 descendants of its own
- K093022: The Picc Wand Peelable Safety Introducer (2010), 31 descendants of its own
- K081697: The Wand Microaccess Safety Introducer, Models 90001, 90002, 90005, 90006 (2008), 27 descendants of its own

Source page: https://510kreport.com/device/K932323
Methodology: https://510kreport.com/methodology