# K071875: V-Cath Poly Picc

- Pathway: 510(k) (Traditional)
- Applicant: Hdc Corp.
- Decided: Nov 5, 2007 after 122 days
- Product code: LJS (Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days)
- Device class: 2
- Regulation: 21 CFR 880.5970
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 8 generations back to K001901 (2000). 23 ancestors in all.
9 later devices descend from it; 2 cite it directly.
2 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K033853: Modification to V-Cath Poly Picc, Hdc Corp. (2004) Summary page 1.
- K051102: Omnipicc PI, Rita Medical Systems, Inc. (2005) Summary page 1.
- K062579: Omnipicc P.I., Rita Medical Systems, Inc. (2006) Summary page 1.
- K033389: Powerpicc Catheters, Models 3175155, 3175135, C.R. Bard, Inc. (2004) Summary page 1.

## Most influential descendants
- 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
- K113622: Orion II CT CVC (2012), 1 descendant of its own

## Indications for use
The Power-V PICC is indicated for patients that require repeated venous access for infusion or injection therapy. The Power-V PICC is indicated for peripheral access to the central venous system for intravenous therapy. The Power-V PICC is indicated for dwell times less than or greater than 30 days. The maximum recommended infusion rate is 5 ml/sec. The maximum pressure of power injectors used with the Power-V PICC catheter may not exceed 300 psi.

Source page: https://510kreport.com/device/K071875
Methodology: https://510kreport.com/methodology