510(k) Report

510(k) · Cleared

Cleared

Patent Hemostasis Band (PH Band)

K201695510(k) TraditionalCleared Oct 30, 2020130-day reviewClass II21 CFR 870.4450

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

Medical Ingenuities · DXC Clamp, Vascular

Cleared on Oct 30, 2020 as substantially equivalent to K162027 (Medtronic Vascular, 2016) after a 130-day review. Its family tree reaches back 2 generations to 2007.

Decided
Oct 30, 2020
Review
130 days
Class
Class II
Product code
DXC
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K070423 (2007). No later device cites it as a predicate yet.

  1. Root · 2 generations backK070423 TR BandTerumo Medical Corp. · 2007
  2. 1 generation backK162027 TRAcelet Compression DeviceMedtronic Vascular · 2016
  3. This deviceK201695 Patent Hemostasis Band (PH Band)Medical Ingenuities · 2020
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K070423TR BandTerumo Medical Corp.2007—
−1K162027TRAcelet Compression DeviceMedtronic Vascular2016—
0 (this device)K201695Patent Hemostasis Band (PH Band)Medical Ingenuities2020—
FIG. 1 — Lineage of K201695, 2007–2020Source: 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 DXC? 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 DXC device

  1. #1 K262086 PreludeSYNC™ Radial Compression Devicescore 13.5 · 7 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
*K162027TRAcelet Compression Device
Summary page 5
…ascular Classification: II Product Code: DXC 510(k) SUMMARY K201695 PREDICATE DEVICE(S) [807.92(a)(3)] Medtronic Vascular TRAcelet Compression Device (K162027) DEVICE DESCRIPTION [807.92(a)(4)] The PH Band, herein referred to as the “Device,” is an compression device consisting of a wri…
Medtronic Vascular2016—
†K070423TR BandTerumo Medical Corp.2007—

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 13 years and passes through 3 companies; a new generation was cleared every 9.6 years on median.
  • None of the 2 ancestors has a recall.

How does its category compare?

All DXC devices

DXC Clamp, Vascular: FDA decisions, review times, recalls and adverse event reports over 20 years. 2020, this device’s year, is highlighted.

FDA decisions per year · DXC

2in 2025

2007: 102008: 32009: 42010: 22011: 62012: 52013: 142014: 42015: 52016: 32017: 32018: 22019: 22020: 32021: 62022: 12023: 42024: 12025: 22026 (partial year): 4
2007high 14 (2013) · low 1 (2022)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DXC

215in 2023

2007: 52 days median2008: 29 days median2009: 83 days median2011: 51 days median2012: 73 days median2013: 89 days median2014: 157 days median2015: 71 days median2016: 91 days median2017: 90 days median2020: 209 days median2021: 37 days median2023: 215 days median2026 (partial year): 125 days median
2007high 215 (2023) · low 29 (2008)2026

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

Recalls per year · DXC

2in 2023

2008: 22009: 22010: 12011: 32014: 12022: 12023: 2
2007high 3 (2011) · low 0 (2007)2026

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

Adverse event reports per year · DXC

442in 2025

2007: 2982008: 3022009: 5392010: 6002011: 6912012: 5482013: 9202014: 4942015: 3742016: 4942017: 4162018: 3912019: 3932020: 4042021: 3712022: 2732023: 6742024: 3752025: 442
2007high 920 (2013) · low 273 (2022)2025

MAUDE reports naming product code DXC, 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
200710520298
20083292302
20094832539
20102—1600
20116513691
20125730548
201314890920
201441571494
20155710374
20163910494
20173900416
20182—0391
20192—0393
202032090404
20216370371
20221—1273
202342152674
20241—0375
20252—0442
202641250—

What is it indicated for?

The PH Band is a compression device used to assist hemostasis of the radial artery after a transradial procedure.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K201695: Patent Hemostasis Band (PH Band).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K201695

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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