# K072196: Angiodynamics, Inc Morpheus Picc and Procedure Kit

- Pathway: 510(k) (Special)
- Applicant: AngioDynamics, Inc.
- Decided: Aug 27, 2007 after 20 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 K041420 (2004). 4 ancestors in all.
6 later devices descend from it; 1 cites it directly.
0 of 11 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041420: Angiodynamics, Inc. Morpheus Picc and Procedure Kit, AngioDynamics, Inc. (2004) Summary page 1.
- K060887: Angiodynamic, Inc. Morpheus CT Picc and Procedure Kit, AngioDynamics, Inc. (2006) Summary page 1.
- K070613: Angiodynamics, Inc., Morpheus CT Picc and Procedure Kit, AngioDynamics, Inc. (2007) Summary page 1.
- K070615: Angiodynamics, Inc., Morpheus CT Picc and Procedure Kit, AngioDynamics, Inc. (2007) Summary page 1.

## Most influential descendants
- K102159: Powerpicc SV Catheters (2010), 5 descendants of its own
- K162443: PowerPICC Provena Catheters (2016), 2 descendants of its own
- K162441: PowerPICC Provena Catheters with SOLO Valve Technology (2017), 1 descendant of its own
- K123617: 3F Pro-Picc (2013), 1 descendant of its own
- K180548: 3F Single Lumen and 4F Dual Lumen PowerPICC Provena Catherers; 3F Single Lumen and 4F Dual Lumen PowerPICC Provena Catherters with SOLO Valve Technology (2018), 0 descendants of its own

## Indications for use
The AngioDynamics, Inc. Morpheus® CT PICC and Procedure Kit is indicated for short or long term peripheral access to the central venous system for intravenous therapy, power injections of contrast media, and allows for central venous pressure monitoring. For blood sampling, infusion, or therapy use a 4 French or larger catheter. For central venous pressure monitoring, it is recommended that catheter lumen of 20 gauge or larger be used.

Source page: https://510kreport.com/device/K072196
Methodology: https://510kreport.com/methodology