# K961155: Solo Picc/Midline Catheter Kit Models 71924, 71908

- Pathway: 510(k) (Traditional)
- Applicant: Douglas Medical Products Corp.
- Decided: Jun 18, 1996 after 88 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 K932211 (1994). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K932211: Procedural Tray for Peripherally Inserted Venous, Pharmacia Deltec, Inc. (1994) Summary page 1.

## Cited in the summary but kept off the family tree
- K083145: Asahi Guide Wire Extension, Model AG149000, Asahi Intecc Co., Ltd. (2009). Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree

## Indications for use
The SoloPak Peripheral Intravenous Catheter Insertion Kits are intended to be used for the placement of a peripheral catheter. The SoloPak Peripheral Intravenous Catheter Insertion Kits include a single lumen catheter, introducer, and the necessary accessories to perform the placement.

Source page: https://510kreport.com/device/K961155
Methodology: https://510kreport.com/methodology