# K062579: Omnipicc P.I.

- Pathway: 510(k) (Traditional)
- Applicant: Rita Medical Systems, Inc.
- Decided: Nov 28, 2006 after 89 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: 7 generations back to K001901 (2000). 21 ancestors in all.
10 later devices descend from it; 2 cite it directly.
2 of 32 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K051102: Omnipicc PI, Rita Medical Systems, Inc. (2005) Summary page 1.
- K033389: Powerpicc Catheters, Models 3175155, 3175135, C.R. Bard, Inc. (2004) Summary page 1.
- K050931: 6 FR DL Powerpicc Catheter, C.R. Bard, Inc. (2005) Summary page 1.
- K051672: Powerpicc, Bard Access Systems, Inc. (2005) Summary page 1.
- K051991: Powerpicc, Poly Per-Q-Cath, 6 FR TL Poly Per-Q-Cath, Power Hohn and Power Line, C.R. Bard, Inc. (2005) Summary page 1.

## 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 OmniPICCPI Peripherally Inserted Central Catheter is indicated for use in attaining short and long term vascular access for administration of medications, parenteral nutrition, IV fluids, blood products or blood withdrawal. The OmniPICCPI is indicated for power injection of contrast media at a maximum recommended infusion rate of 3ml/sec to 5ml/sec and maximum pressure or pounds per square inch (psi) of 300 psi.

Source page: https://510kreport.com/device/K062579
Methodology: https://510kreport.com/methodology