510(k) Report

510(k) · Cleared

Cleared

Hemo-Band

K920614510(k) TraditionalCleared Jul 27, 1992167-day reviewClass II21 CFR 876.5820

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

Innovations IN Access, Inc. · KOC Accessories, Blood Circuit, Hemodialysis

Cleared on Jul 27, 1992 after a 167-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 15 later devices descend from it.

Decided
Jul 27, 1992
Review
167 days
Class
Class II
Product code
KOC
Recalls
None
Predicates
0

15 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2010: 1 descendant cleared2013: 2 descendants cleared2009: 2 descendants cleared2014: 2 descendants cleared2011: 1 descendant cleared2018: 1 descendant cleared2016: 1 descendant cleared2015: 1 descendant cleared2017: 2 descendants cleared2026: 1 descendant cleared1990200020102020
  1. This deviceK920614 Hemo-BandInnovations IN Access, Inc. · 1992
  2. Descendant · cites it directly · 14 of its ownK040208 Neptune Pad, Neptune Disc, Neptune Comfort-Band, Comfort-BandTz Medical, Inc. · 2004 · Recalled
  3. Descendant · 2 generations on · 9 of its ownK092503 Radar Vascular Compression DevicesAdvanced Vascular Dynamics · 2009
  4. Descendant · 3 generations on · 4 of its ownK111837 Radial Artery Compression TourniquetLepu Medical Technology (Beijing) Co., Ltd. · 2011
  5. Descendant · 3 generations on · 3 of its ownK142122 Radar Vascular Compression DeviceAdvanced Vascular Dynamics · 2014
  6. Descendant · 4 generations on · 3 of its ownK142359 Vasc Band hemostatLepu Medical Technology (Beijing) Co., Ltd. · 2014

Showing 5 of 15 descendants. See all descendants

Descendants cleared per year

2004: 12009: 22010: 12011: 12013: 22014: 22015: 12016: 12017: 22018: 12026: 1
2004high 2 (2009) · low 0 (2005)2026

Most influential descendants

Showing 5 of 15 · See all
  • K040208Neptune Pad, Neptune Disc, Neptune Comfort-Band, Comfort-BandTz Medical, Inc. · 2004 · cites it directly14descendants
  • K092503Radar Vascular Compression DevicesAdvanced Vascular Dynamics · 2009 · 2 generations on9descendants
  • K111837Radial Artery Compression TourniquetLepu Medical Technology (Beijing) Co., Ltd. · 2011 · 3 generations on4descendants
  • K142122Radar Vascular Compression DeviceAdvanced Vascular Dynamics · 2014 · 3 generations on3descendants
  • K142359Vasc Band hemostatLepu Medical Technology (Beijing) Co., Ltd. · 2014 · 4 generations on3descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K920614Hemo-BandInnovations IN Access, Inc.1992—
+1K040208Neptune Pad, Neptune Disc, Neptune Comfort-Band, Comfort-BandTz Medical, Inc.20041
+2K092503Radar Vascular Compression DevicesAdvanced Vascular Dynamics2009—
+3K111837Radial Artery Compression TourniquetLepu Medical Technology (Beijing) Co., Ltd.2011—
+3K142122Radar Vascular Compression DeviceAdvanced Vascular Dynamics2014—
+4K142359Vasc Band hemostatLepu Medical Technology (Beijing) Co., Ltd.2014—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200920
201010
201110
201320
201420
201510
201610
201720
201810
202610
FIG. 1 — Lineage of K920614, 1992–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in KOC? 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 KOC device

  1. #1 K230514 Blood Tubing Lines for Hemodialysis AL Series…score 11.8 · 2 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?

FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

What descends from it? (15)

See all 15

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K040208Neptune Pad, Neptune Disc, Neptune Comfort-Band, Comfort-BandTz Medical, Inc.200414

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, K040208 (Tz Medical, Inc., 2004) has gone furthest, with 14 descendants of its own.

How does its category compare?

All KOC devices

KOC Accessories, Blood Circuit, Hemodialysis: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KOC

2in 2025

2007: 12008: 22009: 22012: 12014: 12015: 22016: 12017: 12020: 12023: 22025: 2
2007high 2 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KOC

Too few KOC 510(k)s in any year since 2007 to give a median.

Recalls per year · KOC

4so far in 2026, the most since 2007

2008: 22012: 12014: 12018: 32026 (partial year): 4
2007high 4 (2026) · low 0 (2007)2026

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

Adverse event reports per year · KOC

50in 2025

2007: 32008: 122009: 122010: 42011: 102012: 22013: 222014: 1652015: 5552016: 102017: 232018: 372019: 562020: 202021: 332022: 262023: 162024: 182025: 50
2007high 555 (2015) · low 2 (2012)2025

MAUDE reports naming product code KOC, 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—03
20082—212
20092—012
20100—04
20110—010
20121—12
20130—022
20141—1165
20152—0555
20161—010
20171—023
20180—337
20190—056
20201—020
20210—033
20220—026
20232—016
20240—018
20252—050
20260—4—
Cite this page

510(k) Report. “K920614: Hemo-Band.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K920614

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026