# K060887: Angiodynamic, Inc. Morpheus CT Picc and Procedure Kit

- Pathway: 510(k) (Special)
- Applicant: AngioDynamics, Inc.
- Decided: Apr 28, 2006 after 28 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.
45 later devices descend from it; 4 cite it directly.
1 of 46 devices in its family (counting itself) has 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
- K070002: Boston Scientific Peripherally Inserted Central Catheter (2007), 29 descendants of its own
- K091261: Nmi Picc (2009), 27 descendants of its own
- K101326: NMI IC (2010), 26 descendants of its own
- K093366: Nmi Picc II (2009), 26 descendants of its own
- K121089: Nmi Picc Iii (2012), 23 descendants of its own

## Indications for use
The AngioDynamics, Inc. Morpheus TM 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/K060887
Methodology: https://510kreport.com/methodology