# K132334: Turbo-Ject Peripherally Inserted Central Venous Catheter (Picc) Set

- Pathway: 510(k) (Special)
- Applicant: Cook, Inc.
- Decided: Aug 16, 2013 after 21 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 K072625 (2007). 1 ancestor in all.
2 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K072625: Turbo-Ject Peripherally Inserted Central Venous Catheter (Picc), Cook, Inc. (2007) Summary page 1.

## Most influential descendants
- K141818: Turbo-Ject Picc Sets (2014), 0 descendants of its own
- K133634: Spectrum Turbo-Ject Peripherally Inserted Central Venous Catheter Set (2013), 0 descendants of its own

## Indications for use
Turbo-Ject Peripherally Inserted Central Venous Catheter (P1CC) Sets and Trays are intended for short- or long-term use for venous pressure monitoring, blood sampling, administration of drugs and fluids, and for use with power injectors for delivery of contrast in CT studies. The Turbo- Ject P1CC is indicated for multiple injections of contrast media through a power injector. The maximum pressure limit setting for Power Injectors used with the Turbo-Ject P1CC may not exceed 325 psi and the flow rate may not exceed the maximum flow rate indicated.

Source page: https://510kreport.com/device/K132334
Methodology: https://510kreport.com/methodology