510(k) Report

510(k) · Cleared

Cleared

Compel Surgical Drapes

K923811510(k) TraditionalCleared Feb 23, 1993209-day reviewClass II21 CFR 878.4370

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

Standard Textile Co., Inc. · KKX Drape, Surgical, Antimicrobial

Cleared on Feb 23, 1993 after a 209-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 2 later devices descend from it.

Decided
Feb 23, 1993
Review
209 days
Class
Class II
Product code
KKX
Recalls
None
Predicates
0

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

Descendants, by year cleared 2001: 1 descendant cleared1998: 1 descendant cleared1990200020102020
  1. This deviceK923811 Compel Surgical DrapesStandard Textile Co., Inc. · 1993
  2. Descendant · cites it directly · 0 of its ownK012807 Modification to: Compel Surgical DrapesStandard Textile Co., Inc. · 2001
  3. Descendant · cites it directly · 0 of its ownK980183 Promax Surgical Drapes and CoversStandard Textile Co., Inc. · 1998

Most influential descendants

Showing 2 of 2 · See all
  • K012807Modification to: Compel Surgical DrapesStandard Textile Co., Inc. · 2001 · cites it directly0descendants
  • K980183Promax Surgical Drapes and CoversStandard Textile Co., Inc. · 1998 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K923811Compel Surgical DrapesStandard Textile Co., Inc.1993—
+1K012807Modification to: Compel Surgical DrapesStandard Textile Co., Inc.2001—
+1K980183Promax Surgical Drapes and CoversStandard Textile Co., Inc.1998—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
199810
200110
FIG. 1 — Lineage of K923811, 1993–2001Source: 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 KKX? 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 KKX device

  1. #1 K222578 3M™ Ioban™ CHG Chlorhexidine Gluconate Incise…score 5.7 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

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? (2)

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

NumberDeviceApplicantDecidedDescendants
K012807Modification to: Compel Surgical DrapesStandard Textile Co., Inc.20010
K980183Promax Surgical Drapes and CoversStandard Textile Co., Inc.19980

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, K012807 (Standard Textile Co., Inc., 2001) has gone furthest, with 0 descendants of its own.

How does its category compare?

All KKX devices

KKX Drape, Surgical, Antimicrobial: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · KKX

2in 2023

2007: 42008: 52009: 52010: 82011: 42012: 22013: 32014: 62015: 22017: 12020: 12021: 12023: 2
2007high 8 (2010) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KKX

182in 2014

2007: 181 days median2008: 164 days median2009: 114 days median2010: 107 days median2011: 147 days median2013: 227 days median2014: 182 days median
2007high 227 (2013) · low 107 (2010)2026

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

Recalls per year · KKX

2in 2024

2007: 12010: 12011: 12012: 12013: 72014: 7, 7 Class I2016: 42024: 22026 (partial year): 2
2007high 7 (2013) · low 0 (2008)2026

Class I (7 since 2007) Class II/III not classified

Adverse event reports per year · KKX

24in 2025

2007: 242008: 242009: 272010: 252011: 572012: 402013: 632014: 282015: 332016: 562017: 302018: 322019: 412020: 162021: 412022: 192023: 322024: 192025: 24
2007high 63 (2013) · low 16 (2020)2025

MAUDE reports naming product code KKX, 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
20074181124
20085164024
20095114027
20108107125
20114147157
20122—140
20133227763
201461827 (7)28
20152—033
20160—456
20171—030
20180—032
20190—041
20201—016
20211—041
20220—019
20232—032
20240—219
20250—024
20260—2—
Cite this page

510(k) Report. “K923811: Compel Surgical Drapes.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K923811

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