510(k) · Cleared
ClearedWilson-Cook Biopsy Forceps
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Wilson-Cook Medical, Inc. · KNW Instrument, Biopsy
Cleared on Dec 7, 1987 after a 48-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 4 later devices descend from it.
- Decided
- Dec 7, 1987
- Review
- 48 days
- Class
- Class II
- Product code
- KNW
- Recalls
- None
- Predicates
- 0
4 later devices descend from it, 1 citing it directly.
- This deviceK874314 Wilson-Cook Biopsy ForcepsWilson-Cook Medical, Inc. · 1987
- Descendant · cites it directly · 3 of its ownK953355 Gip/Meid-Globe Hot Biopsy ForcepsMedi-Globe Corp. · 1996
- Descendant · 2 generations on · 2 of its ownK160625 Disposable Hot Biopsy ForcepsMicro-Tech (Nanjing) Co., Ltd. · 2016
- Descendant · 3 generations on · 0 of its ownK173495 Single Use Hot Biopsy Forceps FD-231Olympus Medical Systems Corp. · 2018
- Descendant · 3 generations on · 0 of its ownK180018 Disposable Hot Biopsy ForcepsMicro-Tech (Nanjing) Co., Ltd. · 2018
Most influential descendants
Showing 4 of 4 · See all- K953355Gip/Meid-Globe Hot Biopsy ForcepsMedi-Globe Corp. · 1996 · cites it directly3descendants
- K160625Disposable Hot Biopsy ForcepsMicro-Tech (Nanjing) Co., Ltd. · 2016 · 2 generations on2descendants
- K173495Single Use Hot Biopsy Forceps FD-231Olympus Medical Systems Corp. · 2018 · 3 generations on0descendants
- K180018Disposable Hot Biopsy ForcepsMicro-Tech (Nanjing) Co., Ltd. · 2018 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K874314 | Wilson-Cook Biopsy Forceps | Wilson-Cook Medical, Inc. | 1987 | — |
| +1 | K953355 | Gip/Meid-Globe Hot Biopsy Forceps | Medi-Globe Corp. | 1996 | — |
| +2 | K160625 | Disposable Hot Biopsy Forceps | Micro-Tech (Nanjing) Co., Ltd. | 2016 | — |
| +3 | K173495 | Single Use Hot Biopsy Forceps FD-231 | Olympus Medical Systems Corp. | 2018 | — |
| +3 | K180018 | Disposable Hot Biopsy Forceps | Micro-Tech (Nanjing) Co., Ltd. | 2018 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 2016 | 1 | 0 |
| 2018 | 2 | 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 KNW? 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 KNW device
- #1 K260572 Marrow Marxmanscore 14.5 · 10 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin 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? (4)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K953355 | Gip/Meid-Globe Hot Biopsy Forceps | 1996 | 3 |
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, K953355 (Medi-Globe Corp., 1996) has gone furthest, with 3 descendants of its own.
How does its category compare?
All KNW devicesKNW Instrument, Biopsy: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KNW
12in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KNW
178in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KNW
1in 2024
Class I (4 since 2007) Class II/III not classified
Adverse event reports per year · KNW
1,667in 2025
MAUDE reports naming product code KNW, 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 | 94 | 1 | 766 |
| 2008 | 4 | 53 | 7 | 363 |
| 2009 | 6 | 35 | 3 | 351 |
| 2010 | 3 | 57 | 2 | 162 |
| 2011 | 10 | 64 | 5 | 67 |
| 2012 | 7 | 94 | 1 | 93 |
| 2013 | 3 | 100 | 1 (1) | 98 |
| 2014 | 8 | 95 | 3 | 193 |
| 2015 | 10 | 106 | 0 | 591 |
| 2016 | 9 | 127 | 5 | 297 |
| 2017 | 8 | 90 | 1 | 760 |
| 2018 | 7 | 71 | 0 | 1,012 |
| 2019 | 5 | 94 | 4 | 4,195 |
| 2020 | 8 | 92 | 0 | 5,120 |
| 2021 | 9 | 54 | 3 | 1,020 |
| 2022 | 8 | 203 | 3 | 535 |
| 2023 | 7 | 164 | 2 | 931 |
| 2024 | 5 | 114 | 1 | 1,283 |
| 2025 | 12 | 178 | 0 | 1,667 |
| 2026 | 7 | 29 | 4 (3) | — |
https://510kreport.com/device/K874314 · printed Nov 6, 2026
Cite this page
510(k) Report. “K874314: Wilson-Cook Biopsy Forceps.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K874314
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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