510(k)
K221603: Kangaroo OMNI™ Enteral Feeding Pump (385400);Kangaroo OMNI™ Feeding Set 500ml (B5FD);Kangaroo OMNI™ ENtelliSet 500ml (E5FD);Kangaroo OMNI™ Feeding Set 1000ml (B10FD);Kangaroo OMNI™ ENtelliSet 1000ml (E10FD);Kangaroo OMNI™ ENPlus Spike Set (BSPFD);Kangaroo OMNI™ ENtelliSet ENPlus Spike ( ESPFD);Kangaroo OMNI™ Feeding Set 500ml with Flush Bag ( B5FF);Kangaroo OMNI™ ENtelliSet 500ml with Flush Bag (E5FF);Kangaroo OMNI™ Feeding Set 1000ml with Flush Bag ( E10FF);Kangaroo OMNI™
FDA 510(k) · Cardinal Health, LLC · decided Dec 20, 2022
Key facts
| 510(k) number | K221603 |
|---|---|
| Device name | Kangaroo OMNI™ Enteral Feeding Pump (385400 );Kangaroo OMNI™ Feeding Set 500ml (B5FD );Kangaroo OMNI™ ENtelliSet 500ml (E5FD );Kangaroo OMNI™ Feeding Set 1000ml (B10FD );Kangaroo OMNI™ ENtelliSet 1000ml (E10FD );Kangaroo OMNI™ ENPlus Spike Set (BSPFD );Kangaroo OMNI™ ENtelliSet ENPlus Spike ( ESPFD );Kangaroo OMNI™ Feeding Set 500ml with Flush Bag ( B5FF);Kangaroo OMNI™ ENtelliSet 500ml with Flush Bag (E5FF);Kangaroo OMNI™ Feeding Set 1000ml with Flush Bag ( E10FF );Kangaroo OMNI™ |
| Applicant | Cardinal Health, LLC |
| Product code | LZH |
| Date received | Jun 2, 2022 |
| Decision date | Dec 20, 2022 |
| Decision | Substantially equivalent (SESE) |
| Submission type | Traditional |
| Review panel | General Hospital |
| Medical specialty | General Hospital |
At a glance
- 10–99 MAUDE adverse event reports
- None Recall events
- None UDI device identifiers (GUDID)
- 1–9 Predicate devices cited
- None Later submissions citing this device
- 10–99 510(k)s with this product code
- Yes 510(k) summary on file
- No 510(k) statement on file
- Not listed On the FDA AI-enabled device list
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
Reading a 510(k)
- Decision
- SESE means the FDA found the device substantially equivalent to its predicate, so it may be marketed in the United States.
- Predicates
- Each clearance cites one or more legally marketed devices; the chain of predicates shows where a technology came from.
- Product code
- The three-letter code sets the device type, class and regulation, and groups competing clearances.
- Summary or statement
- Applicants file either a 510(k) summary of the safety and effectiveness information or a statement that it is available on request.
About 510(k) premarket notifications
A 510(k) is a premarket submission made to the FDA to demonstrate that a device is substantially equivalent to a legally marketed predicate device.
Source: U.S. Food and Drug Administration (FDA), 510(k) Premarket Notification database · Source date: