# K012902: Poly Per-Q-Cath Single Lumen Picc Catheter, Model 3143100; Poly Per-Q-Cath Dual Lumen Picc Catheter, Model 3246100

- Pathway: 510(k) (Special)
- Applicant: C.R. Bard, Inc.
- Decided: Sep 10, 2001 after 12 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: 1 generation back to K001901 (2000). 1 ancestor in all.
247 later devices descend from it; 1 cites it directly.
16 of 249 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K001901: Poly Per-Q-Cath Picc Catheter,Model 3236100 and Poly Per-Q-Cath Midline Catheter, Model 3134135, C.R. Bard, Inc. (2000) Summary page 1.

## Most influential descendants
- K031129: Poly Per-Q-Cath Picc Catheters; Poly Radpicc (2003), 246 descendants of its own
- K034019: Poly Per-Q-Cath Picc Catheters (2004), 239 descendants of its own
- K033389: Powerpicc Catheters, Models 3175155, 3175135 (2004), 208 descendants of its own
- K050931: 6 FR DL Powerpicc Catheter (2005), 199 descendants of its own
- K051672: Powerpicc (2005), 178 descendants of its own

## Indications for use
The Poly Per-Q-Cath PICC is indicated for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling. For blood therapy, it is recommended that a 4 French or larger catheter be used.

Source page: https://510kreport.com/device/K012902
Methodology: https://510kreport.com/methodology