# K070613: Angiodynamics, Inc., Morpheus CT Picc and Procedure Kit

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: Jun 29, 2007 after 116 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.
7 later devices descend from it; 1 cites it directly.
0 of 8 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 AngloDynamics, Inc. Morpheus® CT PICC and Procedure Kit is indicated for short or long term peripheral access to the central venous system for intravenous therapy and power injections of contrast media. For blood sampling, infusion, or therapy use a 4 French or larger catheter.

Source page: https://510kreport.com/device/K070613
Methodology: https://510kreport.com/methodology