# K894131: Dermaport Vascular Access Device Model NO. 50-1000

- Pathway: 510(k) (Traditional)
- Applicant: Thermedics, Inc.
- Decided: Sep 26, 1989 after 105 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.
5 later devices descend from it; 2 cite 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K043292: Hemocath (2005), 3 descendants of its own
- K062901: Hemocath II (2007), 2 descendants of its own
- K071202: Dermaport Percutaneous Vascular Access System (Pvas) (2007), 1 descendant of its own
- K091760: Dermaport Ported Vascular Access System (Pvas) (2009), 0 descendants of its own
- K053123: PD Cath (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K894131
Methodology: https://510kreport.com/methodology