# K121094: Medcomp Vascu-Picc & Midline Catheters

- Pathway: 510(k) (Special)
- Applicant: Medical Components, Inc.
- Decided: Jun 6, 2012 after 57 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
No predicates in its family tree.
12 later devices descend from it; 4 cite it directly.
0 of 13 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K141151: CT Midline (2014), 8 descendants of its own
- K153393: PowerMidline Catheter (2016), 5 descendants of its own
- K173114: primeMidline Catheters (2018), 1 descendant of its own
- K162900: PowerMidline Catheter (2016), 1 descendant of its own
- K213203: Provena (TM) Midline Catheter (2022), 0 descendants of its own

## Indications for use
The Peripherally Inserted Central Vein Access catheters are designed for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling, For central venous pressure monitoring (CVP), it is recommended that catheter lumen of 20 gauge or larger be used. The Mdline catheters are indicated for shaft or long term peripheral access to the peripheral veious system for selected intravenous therapies and blood sampling. (See Confraindications). For blood therapy it is recommended that a 4F7rench or larger catheter be used.

Source page: https://510kreport.com/device/K121094
Methodology: https://510kreport.com/methodology