510(k) Report

510(k) · Cleared

Cleared

Nutrac Pelvator, Model Pel 200

K083704510(k) TraditionalCleared Jul 14, 2009211-day reviewClass II21 CFR 876.5320

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

Verity Scientific, Ltd. · KPI Stimulator, Electrical, Non-Implantable, For Incontinence

Cleared on Jul 14, 2009 after a 211-day review. The summary cites one number, which could not be confirmed as its predicate (see the table below). 12 later devices descend from it.

Decided
Jul 14, 2009
Review
211 days
Class
Class II
Product code
KPI
Recalls
None
Predicates
1

12 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2025: 2 descendants cleared2015: 1 descendant cleared2016: 1 descendant cleared2019: 1 descendant cleared2017: 1 descendant cleared2018: 1 descendant cleared2026: 4 descendants cleared2023: 1 descendant cleared20052010201520202025
  1. This deviceK083704 Nutrac Pelvator, Model Pel 200Verity Scientific, Ltd. · 2009
  2. Descendant · cites it directly · 10 of its ownK141643 YarlapInternational Trade Group, Inc. · 2015
  3. Descendant · 2 generations on · 3 of its ownK191312 Perfect PFETenscare, Ltd. · 2019
  4. Descendant · 2 generations on · 2 of its ownK160773 Yarlap IIInternational Trade Group, Inc. · 2016
  5. Descendant · 3 generations on · 0 of its ownK260178 Pelvic Muscle Trainer (KM510, KM516B)Shenzhen Konmed Technology Co., Ltd. · 2026
  6. Descendant · 3 generations on · 0 of its ownK252601 Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L)…Hunan Accurate Bio-Medical Technology Co., Ltd. · 2026

Showing 5 of 12 descendants. See all descendants

Descendants cleared per year

2015: 12016: 12017: 12018: 12019: 12023: 12025: 22026: 4
2015high 4 (2026) · low 0 (2020)2026

Most influential descendants

Showing 5 of 12 · See all
  • K141643YarlapInternational Trade Group, Inc. · 2015 · cites it directly10descendants
  • K191312Perfect PFETenscare, Ltd. · 2019 · 2 generations on3descendants
  • K160773Yarlap IIInternational Trade Group, Inc. · 2016 · 2 generations on2descendants
  • K260178Pelvic Muscle Trainer (KM510, KM516B)Shenzhen Konmed Technology Co., Ltd. · 2026 · 3 generations on0descendants
  • K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle Trainer…Hunan Accurate Bio-Medical Technology Co., Ltd. · 2026 · 3 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K083704Nutrac Pelvator, Model Pel 200Verity Scientific, Ltd.2009—
+1K141643YarlapInternational Trade Group, Inc.2015—
+2K191312Perfect PFETenscare, Ltd.2019—
+2K160773Yarlap IIInternational Trade Group, Inc.2016—
+3K260178Pelvic Muscle Trainer (KM510, KM516B)Shenzhen Konmed Technology Co., Ltd.2026—
+3K252601Pelvic Muscle Trainer (PC22A); Pelvic Muscle Trainer (PC22A-L); Pelvic Muscle…Hunan Accurate Bio-Medical Technology Co., Ltd.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201510
201610
201710
201810
201910
202310
202520
202640
FIG. 1 — Lineage of K083704, 2009–2026Source: 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.

Planning a device in KPI? 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 KPI device

  1. #1 K262353 BTL-299-Fscore 14.8 · 10 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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
Kept off the family treeK018148Kegel8 Pelvic Muscle Trainer
Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree
Summary page 1
…tinence in women 4. Substantial Equivalence The 'NuTracTM Pelvator' Pelvic Muscle Trainer is substantially equivalent to: the "Kegel8" Pelvic Muscle Trainer (K0181480) SECTION 5.0 5. Performance Studies…

What descends from it? (12)

See all 12

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

NumberDeviceApplicantDecidedDescendants
K141643YarlapInternational Trade Group, Inc.201510
K243079NeuroTrac® MyoPlus Pro (MYO120U)Verity Medical, Ltd.20250

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, K141643 (International Trade Group, Inc., 2015) has gone furthest, with 10 descendants of its own.

How does its category compare?

All KPI devices

KPI Stimulator, Electrical, Non-Implantable, For Incontinence: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · KPI

7so far in 2026, the most since 2007

2007: 12008: 12009: 22011: 12012: 22013: 12014: 32015: 62016: 32017: 12018: 32019: 22020: 12021: 32022: 32023: 32024: 42025: 42026 (partial year): 7
2007high 7 (2026) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KPI

263in 2025

2014: 57 days median2015: 260 days median2016: 89 days median2018: 304 days median2021: 217 days median2022: 181 days median2023: 197 days median2024: 172 days median2025: 263 days median2026 (partial year): 248 days median
2007high 304 (2018) · low 57 (2014)2026

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

Recalls per year · KPI

No recall names KPI since 2007.

Adverse event reports per year · KPI

2in 2024

2013: 12015: 22017: 42019: 22020: 32021: 12022: 22023: 62024: 2
2007high 6 (2023) · low 0 (2007)2025

MAUDE reports naming product code KPI, 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
20071—00
20081—00
20092—00
20100—00
20111—00
20122—00
20131—01
201435700
2015626002
201638900
20171—04
2018330400
20192—02
20201—03
2021321701
2022318102
2023319706
2024417202
2025426300
202672480—

What is it indicated for?

The 'NuTraCTM Pelvator' Pelvic Muscle Trainer is intended to provide electrical stimulation and neuromuscular re-education for the purpose of rehabilitation of weak pelvic floor muscles for the treatment of stress urge and :mixed urinary incontinence in women

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K083704: Nutrac Pelvator, Model Pel 200.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K083704

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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