# K123617: 3F Pro-Picc

- Pathway: 510(k) (Traditional)
- Applicant: Medical Components, Inc.
- Decided: May 15, 2013 after 173 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). 34 ancestors in all.
1 later device descends from it; 1 cites it directly.
2 of 36 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 1.
- K091586: Vascu-Picc and Midline Catheters, Single, Double and Triple Lumen, Medcomp (2009) Summary page 1.
- K102159: Powerpicc SV Catheters, C.R. Bard, Inc. (2010) Summary page 1.

## Most influential descendants
- K131687: 6F X 60CM Triple Pro-Line CT Basic IR Set (2013), 0 descendants of its own

## Indications for use
The 3F PRO-PICC, a catheter is indicated for short term or long term peripheral access to the central venous system for intravenous therapy and power injection of contrast media, and allows for central venous pressure monitoring. The maximum recommended infusion rate varies by catheter French size and is printed on the catheter.

Source page: https://510kreport.com/device/K123617
Methodology: https://510kreport.com/methodology