# P010049: Quickseal Femoral Arterial Closure System

- Pathway: PMA
- Applicant: Sub-Q, Inc.
- Decided: Mar 25, 2002 after 196 days
- Product code: MGB (Device, Hemostasis, Vascular)
- Device class: 3
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

## Most influential descendants
- K050135: K-C Hemostatic Biopsy System (2005), 0 descendants of its own

Source page: https://510kreport.com/device/P010049
Methodology: https://510kreport.com/methodology
