510(k) · Cleared
ClearedAngiodynamic, Inc. Morpheus CT Picc and Procedure Kit
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
AngioDynamics, Inc. · LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Cleared on Apr 28, 2006 after a 28-day review. FDA’s file for it is a 510(k) statement, which names no predicate. 1 of the 46 devices in its family, counting itself, has a Class I recall. 45 later devices descend from it.
- Decided
- Apr 28, 2006
- Review
- 28 days
- Class
- Class II
- Product code
- LJS
- Recalls
- None
- Predicates
- 0
45 later devices descend from it, 4 citing it directly. 1 of the 46 devices in this family, counting this one, has a Class I recall.
- This deviceK060887 Angiodynamic, Inc. Morpheus CT Picc and Procedure KitAngioDynamics, Inc. · 2006
- Descendant · cites it directly · 29 of its ownK070002 Boston Scientific Peripherally Inserted Central CatheterBoston Scientific · 2007
- Descendant · 2 generations on · 27 of its ownK091261 Nmi PiccNavilyst Medical, Inc. · 2009 · Recalled
- Descendant · 2 generations on · 26 of its ownK101326 NMI ICNavilyst Medical, Inc. · 2010
- Descendant · 2 generations on · 26 of its ownK093366 Nmi Picc IINavilyst Medical, Inc. · 2009
- Descendant · 2 generations on · 23 of its ownK121089 Nmi Picc IiiNavilyst Medical, Inc. · 2012
Showing 5 of 45 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K131260 Nmi Dialysis Catheter3 generations on · 2014
Most influential descendants
Showing 5 of 45 · See all- K070002Boston Scientific Peripherally Inserted Central CatheterBoston Scientific · 2007 · cites it directly29descendants
- K091261Nmi PiccNavilyst Medical, Inc. · 2009 · 2 generations on27descendants
- K101326NMI ICNavilyst Medical, Inc. · 2010 · 2 generations on26descendants
- K093366Nmi Picc IINavilyst Medical, Inc. · 2009 · 2 generations on26descendants
- K121089Nmi Picc IiiNavilyst Medical, Inc. · 2012 · 2 generations on23descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K060887 | Angiodynamic, Inc. Morpheus CT Picc and Procedure Kit | AngioDynamics, Inc. | 2006 | — |
| +1 | K070002 | Boston Scientific Peripherally Inserted Central Catheter | Boston Scientific | 2007 | — |
| +2 | K091261 | Nmi Picc | Navilyst Medical, Inc. | 2009 | 5 |
| +2 | K101326 | NMI IC | Navilyst Medical, Inc. | 2010 | — |
| +2 | K093366 | Nmi Picc II | Navilyst Medical, Inc. | 2009 | — |
| +2 | K121089 | Nmi Picc Iii | Navilyst Medical, Inc. | 2012 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 2 | 0 |
| 2008 | 1 | 0 |
| 2009 | 3 | 0 |
| 2010 | 4 | 0 |
| 2011 | 1 | 0 |
| 2012 | 4 | 0 |
| 2013 | 6 | 0 |
| 2014 | 3 | 1 |
| 2015 | 5 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2018 | 3 | 0 |
| 2019 | 1 | 0 |
| 2020 | 2 | 0 |
| 2021 | 1 | 0 |
| 2022 | 1 | 0 |
| 2025 | 4 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
1 device in this family has a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new LJS device
- #1 K241910 Neonav ECG Tip Location Systemscore 18.0 · 12 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it? (45)
See all 454 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K131260Nmi Dialysis CatheterNavilyst Medical, Inc. · 2014 · 3 generations on · ◆ in the 2014 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- Of its descendants, K070002 (Boston Scientific, 2007) has gone furthest, with 29 descendants of its own.
How does its category compare?
All LJS devicesLJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · LJS
8in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LJS
171in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LJS
5in 2023
Class I (3 since 2007) Class II/III not classified
Adverse event reports per year · LJS
4,372in 2025
MAUDE reports naming product code LJS, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 14 | 92 | 0 | 392 |
| 2008 | 4 | 97 | 1 | 369 |
| 2009 | 16 | 70 | 1 | 379 |
| 2010 | 9 | 114 | 12 | 495 |
| 2011 | 6 | 55 | 4 | 696 |
| 2012 | 14 | 77 | 40 | 564 |
| 2013 | 14 | 31 | 0 | 680 |
| 2014 | 8 | 47 | 15 | 842 |
| 2015 | 7 | 71 | 2 | 1,306 |
| 2016 | 9 | 128 | 18 | 1,123 |
| 2017 | 7 | 101 | 9 | 2,100 |
| 2018 | 10 | 148 | 3 | 2,324 |
| 2019 | 0 | — | 0 | 2,052 |
| 2020 | 2 | — | 0 | 2,539 |
| 2021 | 3 | 284 | 1 | 3,084 |
| 2022 | 3 | 177 | 0 | 3,256 |
| 2023 | 4 | 47 | 5 (2) | 2,799 |
| 2024 | 1 | — | 0 | 4,243 |
| 2025 | 8 | 171 | 0 | 4,372 |
| 2026 | 2 | — | 8 (1) | — |
What is it indicated for?
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.
Indications for use as stated in the FDA 510(k) statement.
https://510kreport.com/device/K060887 · printed Nov 5, 2026
Cite this page
510(k) Report. “K060887: Angiodynamic, Inc. Morpheus CT Picc and Procedure Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K060887
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026