510(k) · Cleared
ClearedSingle Use Aspiration Needle NA-U200H
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Olympus Medical Systems Corp. · FCG Biopsy Needle
Cleared on Nov 20, 2015 as substantially equivalent to K023272 (The Olympus Optical Co., 2002) and 2 other predicates after a 147-day review. Its family tree reaches back 6 generations to 1990. 3 later devices descend from it.
- Decided
- Nov 20, 2015
- Review
- 147 days
- Class
- Class II
- Product code
- FCG
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 6 generations to K904667 (1990). 9 ancestors in all. 3 later devices descend from it, 2 citing it directly.
- Root · 6 generations backK904667 NA NeedlesOlympus Corp. · 1990
- 5 generations backK973128 Olympus NA-10J-1 Aspiration NeedleOlympus America, Inc. · 1997
- 4 generations backK023272 Disposable Aspiration Needle NA-200HThe Olympus Optical Co. · 2002 · Recalled
- 3 generations backK100712 Resound Endoscopic Ultrasound Aspiration NeedleBoston Scientific Corporation · 2010 · Recalled
- 2 generations backK110030 Expect Endoscopic Aspiration NeedleBoston Scientific Corp · 2011 · Recalled
- 1 generation backK112198 Expect Endoscopic Ultrasound Aspiration NeedleBoston Scientific Corporation · 2011
- This deviceK151738 Single Use Aspiration Needle NA-U200HOlympus Medical Systems Corp. · 2015
- Descendant · cites it directly · 1 of its ownK180449 Single Use Aspiration Needle NA-U200HOlympus Medical Systems Corp. · 2018
- Descendant · 2 generations on · 0 of its ownK252646 Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)Olympus Medical Systems Corp. · 2025
- Descendant · cites it directly · 0 of its ownK181994 Single Use Aspiration Needle NA-U201HOlympus Medical Systems Corp. · 2018
Most influential descendants
Showing 3 of 3 · See all- K180449Single Use Aspiration Needle NA-U200HOlympus Medical Systems Corp. · 2018 · cites it directly1descendant
- K252646Single-Use Fine Needle Biopsy (FNB) device (NA-U210H)Olympus Medical Systems Corp. · 2025 · 2 generations on0descendants
- K181994Single Use Aspiration Needle NA-U201HOlympus Medical Systems Corp. · 2018 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K904667 | NA Needles | Olympus Corp. | 1990 | — |
| −5 | K973128 | Olympus NA-10J-1 Aspiration Needle | Olympus America, Inc. | 1997 | — |
| −4 | K023272 | Disposable Aspiration Needle NA-200H | The Olympus Optical Co. | 2002 | 1 |
| −3 | K100712 | Resound Endoscopic Ultrasound Aspiration Needle | Boston Scientific Corporation | 2010 | 5 |
| −2 | K110030 | Expect Endoscopic Aspiration Needle | Boston Scientific Corp | 2011 | 1 |
| −1 | K112198 | Expect Endoscopic Ultrasound Aspiration Needle | Boston Scientific Corporation | 2011 | — |
| 0 (this device) | K151738 | Single Use Aspiration Needle NA-U200H | Olympus Medical Systems Corp. | 2015 | — |
| +1 | K180449 | Single Use Aspiration Needle NA-U200H | Olympus Medical Systems Corp. | 2018 | — |
| +2 | K252646 | Single-Use Fine Needle Biopsy (FNB) device (NA-U210H) | Olympus Medical Systems Corp. | 2025 | — |
| +1 | K181994 | Single Use Aspiration Needle NA-U201H | Olympus Medical Systems Corp. | 2018 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1993 | 1 | 0 |
| 1994 | 1 | 0 |
| 2000 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2018 | 2 | 0 |
| 2025 | 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 FCG? 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 FCG device
- #1 K250994 ClearTip FNA and FNB Typesscore 13.2 · 12 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 |
|---|---|---|---|
| * | K023272 | Disposable Aspiration Needle NA-200HSummary page 5…e Common Name Applicant 510(k) No. Name Disposable Aspiration OLYMPUS OPTICAL Co., K023272 Aspiration Needle Ltd. Needle NA-200H Olympus Biopsy OLYMPUS AMERICA, INC.… | 2002 |
| * | K973128 | Olympus NA-10J-1 Aspiration NeedleSummary page 5…K023272 Aspiration Needle Ltd. Needle NA-200H Olympus Biopsy OLYMPUS AMERICA, INC. K973128 NA-10J-1 Instruments Aspiration Needle ExpectTM - BOSTON SCIENTIFIC… | 1997 |
| * | K112198 | Expect Endoscopic Ultrasound Aspiration NeedleSummary page 5…ICA, INC. K973128 NA-10J-1 Instruments Aspiration Needle ExpectTM - BOSTON SCIENTIFIC K112198 Endoscopic CORPORATION Aspiration Needle 5.4 Device Description The subject device is a Single Us… | 2011 |
What descends from it? (3)
2 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?
- The line of descent spans 25 years and passes through 6 companies; a new generation was cleared every 5.1 years on median.
- 5 of the 9 ancestors have a recall of any class.
- Of its descendants, K180449 (Olympus Medical Systems Corp., 2018) has gone furthest, with 1 descendant of its own.
- 3 other devices also cite its predicate K023272.
How does its category compare?
All FCG devicesFCG Biopsy Needle: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · FCG
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · FCG
82in 2023
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · FCG
5in 2021
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · FCG
632in 2025
MAUDE reports naming product code FCG, 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 | 4 | 32 | 0 | 11 |
| 2008 | 1 | — | 19 | 115 |
| 2009 | 4 | 87 | 5 | 270 |
| 2010 | 3 | 18 | 4 | 73 |
| 2011 | 1 | — | 2 | 71 |
| 2012 | 0 | — | 0 | 107 |
| 2013 | 1 | — | 0 | 130 |
| 2014 | 5 | 88 | 0 | 154 |
| 2015 | 4 | 91 | 0 | 124 |
| 2016 | 3 | 63 | 0 | 191 |
| 2017 | 3 | 166 | 0 | 273 |
| 2018 | 6 | 140 | 0 | 282 |
| 2019 | 0 | — | 0 | 229 |
| 2020 | 1 | — | 0 | 240 |
| 2021 | 1 | — | 5 | 290 |
| 2022 | 2 | — | 0 | 302 |
| 2023 | 4 | 82 | 0 | 428 |
| 2024 | 1 | — | 0 | 446 |
| 2025 | 2 | — | 0 | 632 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
This instrument has been designed to be used with an Olympus ultrasound endoscope for ultrasonically guided fine needle aspiration (FNA) of submucosal and extramural lesions within the gastrointestinal tract (i.e. pancreatic masses, mediastinal masses, perirectal masses and lymph nodes).
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K151738 · printed Nov 6, 2026
Cite this page
510(k) Report. “K151738: Single Use Aspiration Needle NA-U200H.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151738
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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