510(k) Report

510(k) · Cleared

Cleared

Hemorest (TM)

K864470510(k) TraditionalCleared Jun 23, 1987223-day reviewClass U

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

Health Aid Products · LRL Cushion, Hemorrhoid

Cleared on Jun 23, 1987 after a 223-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jun 23, 1987
Review
223 days
Class
Class U
Product code
LRL
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2007: 1 descendant cleared1990200020102020
  1. This deviceK864470 Hemorest (TM)Health Aid Products · 1987
  2. Descendant · cites it directly · 0 of its ownK072690 Hemaway SeatHemaway, LLC · 2007

Most influential descendants

Showing 1 of 1 · See all
  • K072690Hemaway SeatHemaway, LLC · 2007 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K864470Hemorest (TM)Health Aid Products1987—
+1K072690Hemaway SeatHemaway, LLC2007—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200710
FIG. 1 — Lineage of K864470, 1987–2007Source: 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), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

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What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K072690Hemaway SeatHemaway, LLC20070

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, K072690 (Hemaway, LLC, 2007) has gone furthest, with 0 descendants of its own.

How does its category compare?

All LRL devices

LRL Cushion, Hemorrhoid: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · LRL

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LRL

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

Recalls per year · LRL

No recall names LRL since 2007.

Adverse event reports per year · LRL

No MAUDE report names LRL since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20170—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—
Cite this page

510(k) Report. “K864470: Hemorest (TM).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K864470

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