# K030415: Angiodynamics, Inc. Morpheus Picc and Procedure Kit

- Pathway: 510(k) (Traditional)
- Applicant: AngioDynamics, Inc.
- Decided: Apr 30, 2003 after 82 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: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 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
- K093406: Morpheus Smart Picc CT and Procedure Kit Model 12105509, 12105519 (2010), 0 descendants of its own

## Recalls of this device
- Dec 5, 2011 · Not classified · Z-0467-2012: AngioDynamics distributed the affected PICC catheters that were beyond their expiration date.

## Indications for use
The AngioDynamics, Inc. MorpheusTMPICC and Procedure Kit is indicated for short or long term peripheral access to the central venous system for intravenous therapy and blood sampling.

Source page: https://510kreport.com/device/K030415
Methodology: https://510kreport.com/methodology