510(k) Report

510(k) · Cleared

Cleared

Sterile Repositionable Hemostasis Clipping Device

K152001510(k) TraditionalCleared Dec 10, 2015143-day reviewClass II21 CFR 876.4400

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

Micro-Tech (Nanjing) Co., Ltd. · PKL Hemostatic Metal Clip For The Gi Tract

Cleared on Dec 10, 2015 as substantially equivalent to K122660 (Boston Scientific Corporation, 2012) after a 143-day review. Its family tree reaches back 5 generations to 1997. 15 later devices descend from it.

Decided
Dec 10, 2015
Review
143 days
Class
Class II
Product code
PKL
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K963160 (1997). 15 later devices descend from it, 4 citing it directly.

  1. Root · 5 generations backK963160 HX-5/6-1 Endoscopic Clipping DeviceOlympus America, Inc. · 1997
  2. 4 generations backK990687 HX-5/6-1 Endoscopic Clipping Device, Endoscopic ClipsOlympus Optical, Co. · 1999
  3. 3 generations backK013066 HX-5/6-1 Endoscopic Clipping DeviceOlympus America, Inc. · 2001 · Recalled
  4. 2 generations backK040148 Resolution Hemostasis Clipping DeviceBoston Scientific Corp · 2004 · Recalled
  5. 1 generation backK122660 Resolution Clip Model M00522600, M00522601, M00522602, M00522610…Boston Scientific Corporation · 2012
  6. This deviceK152001 Sterile Repositionable Hemostasis Clipping DeviceMicro-Tech (Nanjing) Co., Ltd. · 2015
  7. Descendant · cites it directly · 13 of its ownK161463 SureClip (TM) Repositionable Hemostasis ClipMicro-Tech (Nanjing) Co., Ltd. · 2017
  8. Descendant · 2 generations on · 8 of its ownK172727 HemoclipHangzhou AGS MedTech Co., Ltd. · 2018
  9. Descendant · 3 generations on · 2 of its ownK211787 HemoclipHangzhou AGS MedTech Co., Ltd. · 2022
  10. Descendant · cites it directly · 1 of its ownK201771 Single Use Rotatable and Repositionable HemoclipAnrei Medical (Hangzhou) Co., Ltd. · 2020
  11. Descendant · cites it directly · 1 of its ownK172762 Single Use HemoclipZhejiang Chuangxiang Medical Technology Co., Ltd. · 2018

Showing 5 of 15 descendants. See all descendants

Descendants cleared per year

2017: 12018: 32020: 12022: 42023: 12024: 32025: 2
2017high 4 (2022) · low 0 (2019)2026

Most influential descendants

Showing 5 of 15 · See all
  • K161463SureClip (TM) Repositionable Hemostasis ClipMicro-Tech (Nanjing) Co., Ltd. · 2017 · cites it directly13descendants
  • K172727HemoclipHangzhou AGS MedTech Co., Ltd. · 2018 · 2 generations on8descendants
  • K211787HemoclipHangzhou AGS MedTech Co., Ltd. · 2022 · 3 generations on2descendants
  • K201771Single Use Rotatable and Repositionable HemoclipAnrei Medical (Hangzhou) Co., Ltd. · 2020 · cites it directly1descendant
  • K172762Single Use HemoclipZhejiang Chuangxiang Medical Technology Co., Ltd. · 2018 · cites it directly1descendant
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K963160HX-5/6-1 Endoscopic Clipping DeviceOlympus America, Inc.1997—
−4K990687HX-5/6-1 Endoscopic Clipping Device, Endoscopic ClipsOlympus Optical, Co.1999—
−3K013066HX-5/6-1 Endoscopic Clipping DeviceOlympus America, Inc.20011
−2K040148Resolution Hemostasis Clipping DeviceBoston Scientific Corp20042
−1K122660Resolution Clip Model M00522600, M00522601, M00522602, M00522610, M00522611…Boston Scientific Corporation2012—
0 (this device)K152001Sterile Repositionable Hemostasis Clipping DeviceMicro-Tech (Nanjing) Co., Ltd.2015—
+1K161463SureClip (TM) Repositionable Hemostasis ClipMicro-Tech (Nanjing) Co., Ltd.2017—
+2K172727HemoclipHangzhou AGS MedTech Co., Ltd.2018—
+3K211787HemoclipHangzhou AGS MedTech Co., Ltd.2022—
+1K201771Single Use Rotatable and Repositionable HemoclipAnrei Medical (Hangzhou) Co., Ltd.2020—
+1K172762Single Use HemoclipZhejiang Chuangxiang Medical Technology Co., Ltd.2018—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201710
201830
202010
202240
202310
202430
202520
FIG. 1 — Lineage of K152001, 1997–2025Source: 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 PKL? 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 PKL device

  1. #1 K202333 Lockado Repositionable Hemostasis Clipscore 17.5 · 7 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
*K122660Resolution Clip Model M00522600, M00522601, M00522602, M00522610, M00522611, M00522612
Summary page 5
…s intended to be used for endoscopic marking, hemostasis for mucosal/submucosal defects in digestive tract. 4. Identification of Predicate Device 510(k) Number: K122660 Product Name: ResolutionTM Hemomstasis Clipping Device 5. Indications for Use The Sterile Repositionable Hemostasis Clip…
Boston Scientific Corporation2012—

Also cleared against K122660: 2 other devices →

What descends from it? (15)

See all 15

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

NumberDeviceApplicantDecidedDescendants
K161463SureClip (TM) Repositionable Hemostasis ClipMicro-Tech (Nanjing) Co., Ltd.201713
K201771Single Use Rotatable and Repositionable HemoclipAnrei Medical (Hangzhou) Co., Ltd.20201
K172762Single Use HemoclipZhejiang Chuangxiang Medical Technology Co., Ltd.20181
K180325Single Use MultiClip DeviceMicro-Tech (Nanjing) Co., Ltd.20180

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 18 years and passes through 5 companies; a new generation was cleared every 2.7 years on median.
  • 2 of the 5 ancestors have a recall of any class.
  • Of its descendants, K161463 (Micro-Tech (Nanjing) Co., Ltd., 2017) has gone furthest, with 13 descendants of its own.
  • 2 other devices also cite its predicate K122660.

How does its category compare?

All PKL devices

PKL Hemostatic Metal Clip For The Gi Tract: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · PKL

6in 2025

2010: 22012: 32013: 22014: 12015: 32016: 12017: 22018: 52019: 42020: 62021: 22022: 92023: 22024: 82025: 62026 (partial year): 7
2007high 9 (2022) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PKL

162in 2025

2012: 102 days median2015: 143 days median2018: 116 days median2019: 231 days median2020: 164 days median2022: 259 days median2024: 181 days median2025: 162 days median2026 (partial year): 231 days median
2007high 259 (2022) · low 102 (2012)2026

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

Recalls per year · PKL

1in 2019

2019: 1
2007high 1 (2019) · low 0 (2007)2026

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

Adverse event reports per year · PKL

1,170in 2025

2012: 12014: 42015: 342016: 1282017: 3982018: 3932019: 6992020: 5042021: 6682022: 5222023: 8632024: 1,2162025: 1,170
2007high 1,216 (2024) · low 0 (2007)2025

MAUDE reports naming product code PKL, 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—00
20080—00
20090—00
20102—00
20110—00
2012310201
20132—00
20141—04
20153143034
20161—0128
20172—0398
201851160393
201942311699
202061640504
20212—0668
202292590522
20232—0863
2024818101,216
2025616201,170
202672310—

What is it indicated for?

The Sterile Repositionable Hemostasis Clipping Device is indicated for endoscopic clip placement within the gastrointestinal tract for the purpose of:

(1) endoscopic marking,

(2) hemostasis for

(a) mucosal / sub-mucosal defects < 3cm,

(b) bleeding ulcers,

(c) polyps < 1.5cm in diameter,

(d) diverticula in the colon,

(3) as a supplementary method, closure of GI tract luminal perforations <20mm that can be treated conservatively.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K152001: Sterile Repositionable Hemostasis Clipping Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K152001

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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