# K070615: Angiodynamics, Inc., Morpheus CT Picc and Procedure Kit

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: May 4, 2007 after 60 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.
8 later devices descend from it; 2 cite it directly.
0 of 9 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
- K072196: Angiodynamics, Inc Morpheus Picc and Procedure Kit (2007), 6 descendants of its own
- 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

## 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/K070615
Methodology: https://510kreport.com/methodology