DEKA Infusion System, DEKA Administration Set (K242693)
Description
DEKA Infusion System, DEKA Administration Set by Deka Research and Development Corporation, an FDA 510(k) cleared general hospital device.
Regulatory Information
FDA Database
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Predicate lineage for K242693
A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. DEKA Infusion System, DEKA Administration Set (K242693) cites 1 predicate device and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K232316 | DEKA Infusion System, DEKA Administration Set | Deka Research and Development | 2024 |
Trace the full predicate network for K242693
A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.