Class Class II
FiAPC plus probes (K242044)
Description
FiAPC plus probes by Erbe Elektromedizin GmbH, an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242044
Clearance Date2024-08-26
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242044
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. FiAPC plus probes (K242044) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K191234 | APC 3 Argon Plasma Coagulation Unit, VIO 3 Electrosurgical ... | Erbe Elektromedizin GmbH | 2019 |
| K060183 | ERBE APC INTEGRATED FILTER PROBES; ERBE APC INTEGRATED FILT... | Erbe USA, Inc. | 2006 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K243451 | FiAPC plus probes | Erbe Elektromedizin GmbH | 2025 |
Trace the full predicate network for K242044
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.