# K033853: Modification to V-Cath Poly Picc

- Pathway: 510(k) (Special)
- Applicant: Hdc Corp.
- Decided: Jan 14, 2004 after 34 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.
10 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K071875: V-Cath Poly Picc (2007), 9 descendants of its own
- K083873: Picc (CT Rated and Non-Rated) (2009), 8 descendants of its own
- K101329: Synergy CT Picc (2010), 6 descendants of its own
- K130034: Uni-Picc (2013), 2 descendants of its own
- K140270: Nexus Midline CT Catheter (2014), 1 descendant of its own

## Indications for use
The V-Cath® Poly PICC is indicated for the patient that requires repeated access for infusion or injection therapy. It can also be used for blood sampling although a 4FR or larger catheter is recommended.

Source page: https://510kreport.com/device/K033853
Methodology: https://510kreport.com/methodology