510(k) · Cleared
ClearedAckermann Europclip
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Ackermann Instrumente GmbH · FZP Clip, Implantable
Cleared on Nov 8, 2011 as substantially equivalent to K053255 (Microsurgical Laboratories,Inc.Dba Wexler Surgical, 2006) and 2 other predicates after a 124-day review. Its family tree reaches back 2 generations to 1998.
- Decided
- Nov 8, 2011
- Review
- 124 days
- Class
- Class II
- Product code
- FZP
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 2 generations to K982313 (1998). 5 ancestors in all, the oldest K830503 (1983). No later device cites it as a predicate yet.
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K982313 | Horizon Titanium Clips, Horizon Tantalum Clips | Weck Closure Systems | 1998 | 1 |
| −1 | K052018 | Miltex Ligating Clip | Miltex, Inc. | 2005 | — |
| 0 (this device) | K111930 | Ackermann Europclip | Ackermann Instrumente GmbH | 2011 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1983 | 1 | 0 |
| 2006 | 1 | 0 |
| 2010 | 1 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FZP? 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 FZP device
- #1 K260677 Vessel Closure Device (VCD177213P)score 12.6 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K053255 | Nexus Ligating ClipSummary page 1…The Europclip is manufactured from commercially pure titanium as described by ISO 5382-2. Predicate Devices: Nexus Ligating Clips (K053255) Miltex Ligating Clips (K052018) Titanium Ligation Clip (K1 00090) Performance Da… | 2006 |
| * | K052018 | Miltex Ligating ClipSummary page 1…y pure titanium as described by ISO 5382-2. Predicate Devices: Nexus Ligating Clips (K053255) Miltex Ligating Clips (K052018) Titanium Ligation Clip (K1 00090) Performance Data: The Europclip functions in the same manner as… | 2005 |
| * | K100090 | Implantable ClipSummary page 1…SO 5382-2. Predicate Devices: Nexus Ligating Clips (K053255) Miltex Ligating Clips (K052018) Titanium Ligation Clip (K1 00090) Performance Data: The Europclip functions in the same manner as the predicates to occlude blood ve… | 2010 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 13 years and passes through 3 companies; a new generation was cleared every 7.2 years on median.
- 2 of the 5 ancestors have a recall of any class.
How does its category compare?
All FZP devicesFZP Clip, Implantable: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.
FDA decisions per year · FZP
5in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FZP
90in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FZP
1in 2020
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FZP
1,902in 2025
MAUDE reports naming product code FZP, 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 | 6 | 31 | 1 | 1,877 |
| 2008 | 4 | 23 | 6 | 981 |
| 2009 | 3 | 22 | 0 | 2,160 |
| 2010 | 6 | 47 | 1 | 2,367 |
| 2011 | 3 | 124 | 0 | 1,678 |
| 2012 | 2 | — | 1 | 1,677 |
| 2013 | 3 | 47 | 0 | 2,381 |
| 2014 | 3 | 29 | 1 | 2,320 |
| 2015 | 8 | 182 | 0 | 2,871 |
| 2016 | 5 | 72 | 2 | 1,840 |
| 2017 | 4 | 29 | 1 | 2,594 |
| 2018 | 4 | 143 | 0 | 2,718 |
| 2019 | 1 | — | 3 | 2,903 |
| 2020 | 2 | — | 1 | 1,760 |
| 2021 | 0 | — | 0 | 1,759 |
| 2022 | 3 | 227 | 0 | 1,575 |
| 2023 | 3 | 65 | 0 | 1,918 |
| 2024 | 2 | — | 0 | 2,067 |
| 2025 | 5 | 90 | 0 | 1,902 |
| 2026 | 2 | — | 0 | — |
What is it indicated for?
The Europolip® is indicated for use in surgical procedures on vessels or other tubular structures where a metal ligating clip is required. The device is intended to occlude the tubular structure by compression.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K111930 · printed Nov 6, 2026
Cite this page
510(k) Report. “K111930: Ackermann Europclip.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K111930
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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