510(k) Report

510(k) · Cleared

Cleared

Single Use Aspiration Needle NA-U201H

K181994510(k) TraditionalCleared Oct 31, 201897-day reviewClass II21 CFR 876.1075

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Olympus Medical Systems Corp. · FCG Biopsy Needle

Cleared on Oct 31, 2018 as substantially equivalent to K151738 (Olympus Medical Systems Corp., 2015) after a 97-day review. Its family tree reaches back 7 generations to 1990.

Decided
Oct 31, 2018
Review
97 days
Class
Class II
Product code
FCG
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K904667 (1990). 10 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 7 generations backK904667 NA NeedlesOlympus Corp. · 1990
  2. 6 generations backK973128 Olympus NA-10J-1 Aspiration NeedleOlympus America, Inc. · 1997
  3. 5 generations backK023272 Disposable Aspiration Needle NA-200HThe Olympus Optical Co. · 2002 · Recalled
  4. 4 generations backK100712 Resound Endoscopic Ultrasound Aspiration NeedleBoston Scientific Corporation · 2010 · Recalled
  5. 3 generations backK110030 Expect Endoscopic Aspiration NeedleBoston Scientific Corp · 2011 · Recalled
  6. 2 generations backK112198 Expect Endoscopic Ultrasound Aspiration NeedleBoston Scientific Corporation · 2011
  7. 1 generation backK151738 Single Use Aspiration Needle NA-U200HOlympus Medical Systems Corp. · 2015
  8. This deviceK181994 Single Use Aspiration Needle NA-U201HOlympus Medical Systems Corp. · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K904667NA NeedlesOlympus Corp.1990—
−6K973128Olympus NA-10J-1 Aspiration NeedleOlympus America, Inc.1997—
−5K023272Disposable Aspiration Needle NA-200HThe Olympus Optical Co.20021
−4K100712Resound Endoscopic Ultrasound Aspiration NeedleBoston Scientific Corporation20105
−3K110030Expect Endoscopic Aspiration NeedleBoston Scientific Corp20111
−2K112198Expect Endoscopic Ultrasound Aspiration NeedleBoston Scientific Corporation2011—
−1K151738Single Use Aspiration Needle NA-U200HOlympus Medical Systems Corp.2015—
0 (this device)K181994Single Use Aspiration Needle NA-U201HOlympus Medical Systems Corp.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
199410
200010
FIG. 1 — Lineage of K181994, 1990–2018Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K250994 ClearTip FNA and FNB Typesscore 13.2 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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.

TypeNumberDeviceApplicantDecidedRecalls
*K151738Single Use Aspiration Needle NA-U200H
Summary page 5
…e NA-U201H Device name 510(k) Submitter 510(k) No. Single Use Aspiration Needle OLYMPUS MEDICAL K151738 NA-U200H SYSTEMS CORP. 2) Reference device Table 12-2 Reference device on Single Use Asp…
Olympus Medical Systems Corp.2015—
†K023272Disposable Aspiration Needle NA-200HThe Olympus Optical Co.20021
†K110030Expect Endoscopic Aspiration NeedleBoston Scientific Corp20111

Also cleared against K151738: 1 other device →

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 28 years and passes through 6 companies; a new generation was cleared every 4.2 years on median.
  • 5 of the 10 ancestors have a recall of any class.
  • 1 other device also cites its predicate K151738.

How does its category compare?

All FCG devices

FCG Biopsy Needle: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · FCG

2in 2025

2007: 42008: 12009: 42010: 32011: 12013: 12014: 52015: 42016: 32017: 32018: 62020: 12021: 12022: 22023: 42024: 12025: 2
2007high 6 (2018) · low 0 (2012)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FCG

82in 2023

2007: 32 days median2009: 87 days median2010: 18 days median2014: 88 days median2015: 91 days median2016: 63 days median2017: 166 days median2018: 140 days median2023: 82 days median
2007high 166 (2017) · low 18 (2010)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · FCG

5in 2021

2008: 192009: 52010: 42011: 22021: 5
2007high 19 (2008) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · FCG

632in 2025

2007: 112008: 1152009: 2702010: 732011: 712012: 1072013: 1302014: 1542015: 1242016: 1912017: 2732018: 2822019: 2292020: 2402021: 2902022: 3022023: 4282024: 4462025: 632
2007high 632 (2025) · low 11 (2007)2025

MAUDE reports naming product code FCG, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
2007432011
20081—19115
20094875270
2010318473
20111—271
20120—0107
20131—0130
20145880154
20154910124
20163630191
201731660273
201861400282
20190—0229
20201—0240
20211—5290
20222—0302
20234820428
20241—0446
20252—0632
20260—0—

What is it indicated for?

These instruments have 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.

Cite this page

510(k) Report. “K181994: Single Use Aspiration Needle NA-U201H.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K181994

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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