510(k) · Cleared
ClearedViky UP
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Endocontrol · LKF Cannula, Manipulator/Injector, Uterine
Cleared on Jun 18, 2013 as substantially equivalent to K082233 (Endocontrol, 2008) and 1 other predicate after a 277-day review. Its family tree reaches back 5 generations to 1993.
- Decided
- Jun 18, 2013
- Review
- 277 days
- Class
- Class II
- Product code
- LKF
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 5 generations to K931783 (1993). 9 ancestors in all. No later device cites it as a predicate yet.
- Root · 5 generations backK931783 Aesop (Automated Endoscopic System for Optimal PosComputer Motion, Inc. · 1993
- 4 generations backK960655 Aesop System and AccessoriesComputer Motion, Inc. · 1996
- 3 generations backK963126 Aesop System and AccessoriesComputer Motion, Inc. · 1997
- 2 generations backK972699 Aesop 3000 System and AccessoriesComputer Motion, Inc. · 1997
- 1 generation backK082233 VIKYEndocontrol · 2008
- This deviceK122820 Viky UPEndocontrol · 2013
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −5 | K931783 | Aesop (Automated Endoscopic System for Optimal Pos | Computer Motion, Inc. | 1993 | — |
| −4 | K960655 | Aesop System and Accessories | Computer Motion, Inc. | 1996 | — |
| −3 | K963126 | Aesop System and Accessories | Computer Motion, Inc. | 1997 | — |
| −2 | K972699 | Aesop 3000 System and Accessories | Computer Motion, Inc. | 1997 | — |
| −1 | K082233 | VIKY | Endocontrol | 2008 | — |
| 0 (this device) | K122820 | Viky UP | Endocontrol | 2013 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1995 | 1 | 0 |
| 2004 | 1 | 0 |
| 2005 | 1 | 0 |
| 2007 | 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 LKF? 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 LKF device
- #1 K241693 FemChec Controlled Saline-Air Device (FCD-250)score 11.6 · 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? (2)
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 |
|---|---|---|---|
| * | K082233 | VIKYSummary page 1…Positioner, Arm * Regulation number Unclassified Regulation name Unclassified Regulatory class Unclassified Product code LKF Predicate devices e ViKY Endoscope Holder (K082233), EndoControl s Probe Holder System (K071405), Intuitive Surgical Purpose The purpose of this 510{k) submission is fo demonstrat… | 2008 |
| * | K071405 | Probe Holder SystemSummary page 1…fied Regulation name Unclassified Regulatory class Unclassified Product code LKF Predicate devices e ViKY Endoscope Holder (K082233), EndoControl s Probe Holder System (K071405), Intuitive Surgical Purpose The purpose of this 510{k) submission is fo demonstrate that the subject dewce is substantially equ… | 2007 |
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 20 years and passes through 2 companies; a new generation was cleared every 2.4 years on median.
- None of the 9 ancestors has a recall.
How does its category compare?
All LKF devicesLKF Cannula, Manipulator/Injector, Uterine: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · LKF
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · LKF
136in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · LKF
3in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · LKF
95in 2025
MAUDE reports naming product code LKF, 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 | 3 | 141 | 0 | 36 |
| 2008 | 0 | — | 2 | 59 |
| 2009 | 2 | — | 0 | 53 |
| 2010 | 6 | 178 | 0 | 46 |
| 2011 | 3 | 187 | 0 | 98 |
| 2012 | 0 | — | 2 | 104 |
| 2013 | 3 | 266 | 0 | 53 |
| 2014 | 3 | 169 | 0 | 45 |
| 2015 | 5 | 140 | 0 | 53 |
| 2016 | 1 | — | 0 | 62 |
| 2017 | 1 | — | 0 | 64 |
| 2018 | 4 | 267 | 0 | 23 |
| 2019 | 1 | — | 0 | 76 |
| 2020 | 0 | — | 0 | 119 |
| 2021 | 0 | — | 0 | 189 |
| 2022 | 4 | 79 | 3 | 100 |
| 2023 | 0 | — | 0 | 88 |
| 2024 | 3 | 136 | 0 | 125 |
| 2025 | 2 | — | 0 | 95 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The VIKY UP device is indicated for computer-controlled laparoscopic hysterectomies (such as da Vinci-assisted laparoscopic hysterectomies) for the purpose of holding and controlling the movement of a uterine manipulator.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K122820 · printed Nov 6, 2026
Cite this page
510(k) Report. “K122820: Viky UP.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K122820
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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