# K003753: GP General Purpose Drainage Set, Mini-Pigtail Drainage Catheter with Locking Pigtail, GP General Purpose Drainage  Cathe

- Pathway: 510(k) (Special)
- Applicant: Uresil Corp.
- Decided: Jan 4, 2001 after 30 days
- Product code: FGE (Stents, Drains And Dilators For The Biliary Ducts)
- Device class: 2
- Regulation: 21 CFR 876.5010
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 1 cites it directly.
0 of 6 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
- K033862: Bioteq Pigtail Drainage Catheter Set (One Step Type) with or Without Safety String Lock (2005), 4 descendants of its own
- K200103: BIOTEQ Drainage Catheter Set (One Step Type) (2020), 3 descendants of its own
- K210419: BIOTEQ Drainage Catheter BT-PDS-series (2022), 2 descendants of its own
- K254179: Drainage Catheter (2026), 0 descendants of its own
- K251019: BIOTEQ Drainage Catheter Set: BT-PD1-SERIES-G and BT-PDS-SERIES-G (2025), 0 descendants of its own

Source page: https://510kreport.com/device/K003753
Methodology: https://510kreport.com/methodology