510(k) Report

510(k) · Cleared

Cleared

SpyScope DS Access and Delivery Catheter, SpyScope DS II Access and Delivery Catheter, SpyGlass DS Digital Controller

K183636510(k) SpecialCleared Jan 22, 201927-day reviewClass II21 CFR 876.1500

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

Boston Scientific Corporation · FBN Choledochoscope And Accessories, Flexible/Rigid

Cleared on Jan 22, 2019 as substantially equivalent to K181439 (Boston Scientific Corporation, 2018) after a 27-day review. Its family tree reaches back 9 generations to 1993. 2 of the 48 devices in its family, counting itself, have a Class I recall. 5 later devices descend from it.

Decided
Jan 22, 2019
Review
27 days
Class
Class II
Product code
FBN
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K931154 (1993). 42 ancestors in all, the oldest K843084 (1985). 5 later devices descend from it, 2 citing it directly. 2 of the 48 devices in this family, counting this one, have a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2009: 1 other ancestor2008: 2 other ancestors2005: 4 other ancestors2003: 3 other ancestors, 1 with a Class I recall12001: 4 other ancestors1999: 1 other ancestor1996: 1 other ancestor1997: 3 other ancestors1995: 5 other ancestors1991: 4 other ancestors, 1 with a Class I recall12000: 1 other ancestor1993: 1 other ancestor1992: 1 other ancestor1985: 2 other ancestors2026: 3 descendants cleared2020: 1 descendant cleared2023: 1 descendant clearedK931154 · Evis 200 System · Olympus Corp. · 1993K963033 · BF 240/P240/IT240 Bronchovideoscope & Accessories · Olympus America, Inc. · 1996 · recalledK981543 · Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and Ancillary Equipment · The Olympus Optical Co. · 1998 · recalledK021074 · Visera Cystovideoscope Olympus Cyf Type V/VA · Olympus America, Inc. · 2002K030960 · Ecn Electronic Video Cystonephroscope · Acmi Corporation · 2003K042225 · Acmi Invisio Icn, Models Icn-0564 and Icn-0565 · Acmi Corporation · 2004K060269 · Acmi Dur-Digital Ureteroscope and Choledochoscope System · Acmi Corporation · 2006K142922 · SpyGlass DS Direct Visualization System · Boston Scientific Corporation · 2015 · recalledK181439 · SpyGlass DS and DS II Direct Visualization System · Boston Scientific Corporation · 20181990200020102020
  1. Root · 9 generations backK931154 Evis 200 SystemOlympus Corp. · 1993
  2. 5 generations between
  3. 3 generations backK060269 Acmi Dur-Digital Ureteroscope and Choledochoscope SystemAcmi Corporation · 2006
  4. 2 generations backK142922 SpyGlass DS Direct Visualization SystemBoston Scientific Corporation · 2015 · Recalled
  5. 1 generation backK181439 SpyGlass DS and DS II Direct Visualization SystemBoston Scientific Corporation · 2018
  6. This deviceK183636 SpyScope DS Access and Delivery Catheter, SpyScope DS II Access and…Boston Scientific Corporation · 2019
  7. Descendant · cites it directly · 3 of its ownK200483 SpyGlass Discover Digital Catheter, SpyGlass Discover Digital…Boston Scientific Corporation · 2020
  8. Descendant · 2 generations on · 2 of its ownK221784 Single-use Video Pancreaticobiliary Scope, PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2023
  9. Descendant · 3 generations on · 0 of its ownK252492 Visualized Access and Delivery Catheter; PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2026
  10. Descendant · 3 generations on · 0 of its ownK254153 Single-use Video Scope; PB Digital ControllerMirco-Tech (Nanjing) Co., Ltd. · 2026
  11. Descendant · cites it directly · 0 of its ownK251338 Cholangioscope Visualization System (Single-use Video…Scivita Medical Technology Co., Ltd. · 2026
Show all 9 generations
  1. Root · 9 generations backK931154 Evis 200 SystemOlympus Corp. · 1993
  2. 8 generations backK963033 BF 240/P240/IT240 Bronchovideoscope & AccessoriesOlympus America, Inc. · 1996 · Recalled
  3. 7 generations backK981543 Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories…The Olympus Optical Co. · 1998 · Recalled
  4. 6 generations backK021074 Visera Cystovideoscope Olympus Cyf Type V/VAOlympus America, Inc. · 2002
  5. 5 generations backK030960 Ecn Electronic Video CystonephroscopeAcmi Corporation · 2003
  6. 4 generations backK042225 Acmi Invisio Icn, Models Icn-0564 and Icn-0565Acmi Corporation · 2004
  7. 3 generations backK060269 Acmi Dur-Digital Ureteroscope and Choledochoscope SystemAcmi Corporation · 2006
  8. 2 generations backK142922 SpyGlass DS Direct Visualization SystemBoston Scientific Corporation · 2015 · Recalled
  9. 1 generation backK181439 SpyGlass DS and DS II Direct Visualization SystemBoston Scientific Corporation · 2018
  10. This deviceK183636 SpyScope DS Access and Delivery Catheter, SpyScope DS II Access and…Boston Scientific Corporation · 2019

Class I recalls in this family

Most influential descendants

Showing 5 of 5 · See all
  • K200483SpyGlass Discover Digital Catheter, SpyGlass Discover Digital ControllerBoston Scientific Corporation · 2020 · cites it directly3descendants
  • K221784Single-use Video Pancreaticobiliary Scope, PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2023 · 2 generations on2descendants
  • K252492Visualized Access and Delivery Catheter; PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd. · 2026 · 3 generations on0descendants
  • K254153Single-use Video Scope; PB Digital ControllerMirco-Tech (Nanjing) Co., Ltd. · 2026 · 3 generations on0descendants
  • K251338Cholangioscope Visualization System (Single-use Video Cholangioscope: SCV-P-01G…Scivita Medical Technology Co., Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K931154Evis 200 SystemOlympus Corp.1993—
−8K963033BF 240/P240/IT240 Bronchovideoscope & AccessoriesOlympus America, Inc.19966
−7K981543Olympus LF-TP and LF-DP Tracheal Intubation Fiberscopes, Accessories and…The Olympus Optical Co.19985
−6K021074Visera Cystovideoscope Olympus Cyf Type V/VAOlympus America, Inc.2002—
−5K030960Ecn Electronic Video CystonephroscopeAcmi Corporation2003—
−4K042225Acmi Invisio Icn, Models Icn-0564 and Icn-0565Acmi Corporation2004—
−3K060269Acmi Dur-Digital Ureteroscope and Choledochoscope SystemAcmi Corporation2006—
−2K142922SpyGlass DS Direct Visualization SystemBoston Scientific Corporation20151
−1K181439SpyGlass DS and DS II Direct Visualization SystemBoston Scientific Corporation2018—
0 (this device)K183636SpyScope DS Access and Delivery Catheter, SpyScope DS II Access and Delivery…Boston Scientific Corporation2019—
+1K200483SpyGlass Discover Digital Catheter, SpyGlass Discover Digital ControllerBoston Scientific Corporation2020—
+2K221784Single-use Video Pancreaticobiliary Scope, PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd.2023—
+3K252492Visualized Access and Delivery Catheter; PB Digital ControllerMicro-Tech (Nanjing) Co., Ltd.2026—
+3K254153Single-use Video Scope; PB Digital ControllerMirco-Tech (Nanjing) Co., Ltd.2026—
+1K251338Cholangioscope Visualization System (Single-use Video Cholangioscope…Scivita Medical Technology Co., Ltd.2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198520
199141
199210
199310
199550
199610
199730
199910
200010
200140
200331
200540
200820
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202010
202310
202630
FIG. 1 — Lineage of K183636, 1993–2026Source: 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.

2 devices in this family have a Class I recall. 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 FBN device

  1. #1 K254153 Single-use Video Scope; PB Digital Controllerscore 14.4 · 12 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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
*K181439SpyGlass DS and DS II Direct Visualization System
Summary page 4
…SpyGlass DS and DS II Direct Visualization System Manufacturer: Boston Scientific Corporation Clearance Number: K181439 Common Name: Choledochoscope and accessories, flexible/rigid; Surgical…
Boston Scientific Corporation2018—

Also cleared against K181439: 1 other device →

What descends from it? (5)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K200483SpyGlass Discover Digital Catheter, SpyGlass Discover Digital ControllerBoston Scientific Corporation20203
K251338Cholangioscope Visualization System (Single-use Video Cholangioscope: SCV-P-01G…Scivita Medical Technology Co., Ltd.20260

Has anything in its family been recalled? (2 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K023984Modification to Olympus Bronchoscopes BF-40 Series, BF-240 Series, and BF-160 SeriesThe Olympus Optical Co. · 2003 · 6 generations back · ◆ in the 2003 ancestors bar of FIG. 114 Class I recalls
  • K912120Urf-P2 Ureterorenofiberscope/CholedochofiberscopeOlympus Corp. · 1991 · 7 generations back · ◆ in the 1991 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 26 years and passes through 5 companies; a new generation was cleared every 1.7 years on median.
  • 16 of the 42 ancestors have a recall of any class; 2 have a Class I recall.
  • Of its descendants, K200483 (Boston Scientific Corporation, 2020) has gone furthest, with 3 descendants of its own.
  • 1 other device also cites its predicate K181439.

How does its category compare?

All FBN devices

FBN Choledochoscope And Accessories, Flexible/Rigid: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, this device’s year, is highlighted.

FDA decisions per year · FBN

3in 2025

2008: 32010: 12012: 12015: 12016: 12018: 12019: 12020: 12023: 42024: 22025: 32026 (partial year): 3
2007high 4 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FBN

150in 2025

2008: 64 days median2023: 215 days median2025: 150 days median2026 (partial year): 175 days median
2007high 215 (2023) · low 64 (2008)2026

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

Recalls per year · FBN

1in 2024

2020: 12023: 12024: 1, 1 Class I2026 (partial year): 1
2007high 1 (2020) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · FBN

118in 2025

2007: 12008: 52009: 42010: 22011: 22013: 22014: 22015: 22016: 1682017: 2242018: 6392019: 1052020: 1732021: 1582022: 2832023: 1052024: 1072025: 118
2007high 639 (2018) · low 0 (2012)2025

MAUDE reports naming product code FBN, 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
20070—01
200836405
20090—04
20101—02
20110—02
20121—00
20130—02
20140—02
20151—02
20161—0168
20170—0224
20181—0639
20191—0105
20201—1173
20210—0158
20220—0283
202342151105
20242—1 (1)107
202531500118
202631751—

What is it indicated for?

The SpyGlass DS and DS II Direct Visualization System is indicated for use in diagnostic and therapeutic applications during endoscopic procedures in the pancreatico-biliary system including the hepatic ducts. The SpyGlass DS and DS II Direct Visualization System comprises two components: the SpyScope DS Access and Delivery Catheter or SpyScope DS II Access and Delivery Catheter, and the SpyGlass DS Digital Controller. The SpyScope DS Access and Delivery…

Read the full statement (155 words)

The SpyGlass DS and DS II Direct Visualization System is indicated for use in diagnostic and therapeutic applications during endoscopic procedures in the pancreatico-biliary system including the hepatic ducts.

The SpyGlass DS and DS II Direct Visualization System comprises two components: the SpyScope DS Access and Delivery Catheter or SpyScope DS II Access and Delivery Catheter, and the SpyGlass DS Digital Controller.

The SpyScope DS Access and Delivery Catheter and SpyScope DS II Access and Delivery Catheter are intended to provide direct visualization and to guide both optical and accessory devices for diagnostic and therapeutic applications during endoscopic procedures in the pancreatico-biliary system including the hepatic ducts.

The SpyGlass DS Digital Controller is intended to provide illumination and receive, process, and output images from the SpyScope DS Access and Delivery Catheter or SpyScope DS II Access and Delivery Catheter for diagnostic and therapeutic applications during endoscopic procedures in the pancreaticobiliary system including the hepatic ducts.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K183636: SpyScope DS Access and Delivery Catheter, SpyScope DS II Access and Delivery Catheter, SpyGlass DS Digital Controller.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K183636

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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