510(k) Report

510(k) · Cleared

Cleared

CP&S Disposable Instant Cold Compress

K890553510(k) TraditionalCleared Feb 13, 19897-day reviewClass I21 CFR 890.5710

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

Consolidated Products & Services, Inc. · IMD Pack, Hot Or Cold, Disposable

Cleared on Feb 13, 1989 after a 7-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
Feb 13, 1989
Review
7 days
Class
Class I
Product code
IMD
Recalls
None
Predicates
0

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

Descendants, by year cleared 1997: 1 descendant cleared1990200020102020
  1. This deviceK890553 CP&S Disposable Instant Cold CompressConsolidated Products & Services, Inc. · 1989
  2. Descendant · cites it directly · 0 of its ownK974190 CP&S Instant Cold Pack Limb Kit TransporterConsolidated Products & Services, Inc. · 1997

Most influential descendants

Showing 1 of 1 · See all
  • K974190CP&S Instant Cold Pack Limb Kit TransporterConsolidated Products & Services, Inc. · 1997 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K890553CP&S Disposable Instant Cold CompressConsolidated Products & Services, Inc.1989—
+1K974190CP&S Instant Cold Pack Limb Kit TransporterConsolidated Products & Services, Inc.1997—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199710
FIG. 1 — Lineage of K890553, 1989–1997Source: 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.

Planning a device in IMD? 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 IMD device

  1. #1 K221653 InfaTherm Disposable Infant Warming Mattressscore 4.4 · 2 generations · no Class I recall
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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
K974190CP&S Instant Cold Pack Limb Kit TransporterConsolidated Products & Services, Inc.19970

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, K974190 (Consolidated Products & Services, Inc., 1997) has gone furthest, with 0 descendants of its own.

How does its category compare?

All IMD devices

IMD Pack, Hot Or Cold, Disposable: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · IMD

1in 2022

2007: 12008: 12012: 12017: 12022: 1
2007high 1 (2007) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · IMD

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

Recalls per year · IMD

4in 2021

2008: 42010: 12015: 12018: 32021: 4
2007high 4 (2008) · low 0 (2007)2026

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

Adverse event reports per year · IMD

66in 2025

2007: 2112008: 8042009: 2102010: 582011: 702012: 532013: 402014: 332015: 1932016: 2132017: 2342018: 2622019: 6322020: 2482021: 1422022: 2022023: 1842024: 1122025: 66
2007high 804 (2008) · low 33 (2014)2025

MAUDE reports naming product code IMD, 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—0211
20081—4804
20090—0210
20100—158
20110—070
20121—053
20130—040
20140—033
20150—1193
20160—0213
20171—0234
20180—3262
20190—0632
20200—0248
20210—4142
20221—0202
20230—0184
20240—0112
20250—066
20260—0—
Cite this page

510(k) Report. “K890553: CP&S Disposable Instant Cold Compress.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K890553

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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