# K141633: Pro-Picc with Valve Technology

- Pathway: 510(k) (Traditional)
- Applicant: Medical Components, Inc.
- Decided: Sep 29, 2014 after 103 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: 9 generations back to K001901 (2000). 32 ancestors in all.
No later device cites it as a predicate yet.
2 of 33 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K091953: Pro-Picc, Medcomp (2009) Summary page 4.
- K092347: Pro-Picc CT, Medcomp (2009) Summary page 4.
- K072230: Powerpicc Solo, C.R. Bard, Inc. (2007) Summary page 4.

## Indications for use
The Pro-PICC catheter with valve technology is indicated for short and long peripheral access to the central venous system for intravenous therapy and power injection media, and allow for central venous pressure monitoring. For blood sampling, infusion, or therapies, use a 4F or larger catheter. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter.

Source page: https://510kreport.com/device/K141633
Methodology: https://510kreport.com/methodology