510(k) · Cleared
ClearedMicro Link Endoscopic Fiber Cable, Model B1-90159
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Cogent Light Technologies, Inc. · FFS Image, Illumination, Fiberoptic, For Endoscope
Cleared on Jul 17, 2000 after a 45-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 3 later devices descend from it.
- Decided
- Jul 17, 2000
- Review
- 45 days
- Class
- Class II
- Product code
- FFS
- Recalls
- None
- Predicates
- 0
3 later devices descend from it, 3 citing it directly.
- This deviceK001698 Micro Link Endoscopic Fiber Cable, Model B1-90159Cogent Light Technologies, Inc. · 2000
- Descendant · cites it directly · 0 of its ownK061622 PS SeriesPhotonic Optische Gerate Gesmbh & Cokg · 2007
- Descendant · cites it directly · 0 of its ownK070287 PS Series with Fiber Light Guide and Headlight, Models PS200, PS250…Photonic Optische Gerate GmbH & Cokg · 2007
- Descendant · cites it directly · 0 of its ownK063309 Tru-CableTruphatek International, Ltd. · 2007
Most influential descendants
Showing 3 of 3 · See all- K061622PS SeriesPhotonic Optische Gerate Gesmbh & Cokg · 2007 · cites it directly0descendants
- K070287PS Series with Fiber Light Guide and Headlight, Models PS200, PS250, PS500Photonic Optische Gerate GmbH & Cokg · 2007 · cites it directly0descendants
- K063309Tru-CableTruphatek International, Ltd. · 2007 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K001698 | Micro Link Endoscopic Fiber Cable, Model B1-90159 | Cogent Light Technologies, Inc. | 2000 | — |
| +1 | K061622 | PS Series | Photonic Optische Gerate Gesmbh & Cokg | 2007 | — |
| +1 | K070287 | PS Series with Fiber Light Guide and Headlight, Models PS200, PS250, PS500 | Photonic Optische Gerate GmbH & Cokg | 2007 | — |
| +1 | K063309 | Tru-Cable | Truphatek International, Ltd. | 2007 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2007 | 3 | 0 |
Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in FFS? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
What was it cleared against?
FDA has not posted a summary or statement for it, so its predicates are not known.
What descends from it? (3)
3 later devices cite it directly; ranked here by how many devices descend from each in turn.
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?
- Of its descendants, K061622 (Photonic Optische Gerate Gesmbh & Cokg, 2007) has gone furthest, with 0 descendants of its own.
How does its category compare?
All FFS devicesFFS Image, Illumination, Fiberoptic, For Endoscope: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · FFS
3in 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · FFS
74in 2007
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FFS
1in 2007
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FFS
5in 2024
MAUDE reports naming product code FFS, 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 | 74 | 1 | 12 |
| 2008 | 0 | — | 0 | 17 |
| 2009 | 0 | — | 0 | 14 |
| 2010 | 0 | — | 0 | 5 |
| 2011 | 0 | — | 0 | 7 |
| 2012 | 0 | — | 0 | 4 |
| 2013 | 0 | — | 0 | 10 |
| 2014 | 0 | — | 0 | 5 |
| 2015 | 0 | — | 0 | 4 |
| 2016 | 0 | — | 0 | 7 |
| 2017 | 0 | — | 0 | 19 |
| 2018 | 0 | — | 0 | 19 |
| 2019 | 0 | — | 0 | 17 |
| 2020 | 0 | — | 0 | 56 |
| 2021 | 0 | — | 0 | 57 |
| 2022 | 0 | — | 0 | 10 |
| 2023 | 0 | — | 0 | 6 |
| 2024 | 0 | — | 0 | 5 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K001698 · printed Nov 6, 2026
Cite this page
510(k) Report. “K001698: Micro Link Endoscopic Fiber Cable, Model B1-90159.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K001698
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Record history
- FDA decision record loaded May 2, 2026
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026