510(k) Report

510(k) · Cleared

Recalled · Class II · 2024

3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing

K171908510(k) SpecialCleared Jul 11, 201715-day reviewClass URecalls 1

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

3M Company · SEL Securement Wound Dressing For Reduction Of Infection

Cleared on Jul 11, 2017 as substantially equivalent to K063458 (3M Company, 2007) and 2 other predicates after a 15-day review. Its family tree reaches back 5 generations to 1991. It has been recalled once.

Decided
Jul 11, 2017
Review
15 days
Class
Class U
Product code
SEL
Recalls
1
Predicates
3

Its longest line of descent runs back 5 generations to K895920 (1991). 8 ancestors in all, the oldest K895207 (1989). No later device cites it as a predicate yet.

  1. Root · 5 generations backK895920 Vitapatch Pin Protection Device for PercutaneousVitaphore Corp. · 1991
  2. 4 generations backK003229 Biopatch Antimicrobial DressingIntegra Lifesciences Corp. · 2001
  3. 3 generations backK063458 3M Tegaderm CHG Dressing3M Company · 2007 · Recalled
  4. 2 generations backK080620 Modification to 3M Tegaderm CHG Dressing3M Company-3M Health Care · 2008 · Recalled
  5. 1 generation backK153410 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing3M Company · 2017 · Recalled
  6. This deviceK171908 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing3M Company · 2017
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K895920Vitapatch Pin Protection Device for PercutaneousVitaphore Corp.1991—
−4K003229Biopatch Antimicrobial DressingIntegra Lifesciences Corp.2001—
−3K0634583M Tegaderm CHG Dressing3M Company20071
−2K080620Modification to 3M Tegaderm CHG Dressing3M Company-3M Health Care20081
−1K1534103M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing3M Company20171
0 (this device)K1719083M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing3M Company2017—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198920
199710
FIG. 1 — Lineage of K171908, 1991–2017Source: 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 SEL? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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What was it cleared against? (3)

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
*K0634583M Tegaderm CHG Dressing
Summary page 5
…510(k) Premarket Notification – Special 510(k): Device Modification III. PREDICATE DEVICE 3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Securement Dressing (K063458, K080620, K153410) No reference devices are used in this submission. IV. DEVICE DESCRIPTION 3M™ Tegaderm™ CHG Chlorhexidine Glu…
3M Company20071
*K080620Modification to 3M Tegaderm CHG Dressing
Summary page 5
…510(k) Premarket Notification – Special 510(k): Device Modification III. PREDICATE DEVICE 3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Securement Dressing (K063458, K080620, K153410) No reference devices are used in this submission. IV. DEVICE DESCRIPTION 3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.…
3M Company-3M Health Care20081
*K1534103M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing
Summary page 5
…remarket Notification – Special 510(k): Device Modification III. PREDICATE DEVICE 3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Securement Dressing (K063458, K080620, K153410) No reference devices are used in this submission. IV. DEVICE DESCRIPTION 3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Secure…
3M Company20171

Also cleared against K063458: 5 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

Recalls of this device

DateClassRecallRoot causeReason
Aug 14, 2024Class IIZ-0038-2025Under Investigation by firmContamination with foreign substance matter

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 26 years and passes through 4 companies; a new generation was cleared every 5.4 years on median.
  • 3 of the 8 ancestors have a recall of any class.
  • 5 other devices also cite its predicate K063458.

How does its category compare?

All SEL devices

SEL Securement Wound Dressing For Reduction Of Infection: FDA decisions, review times, recalls and adverse event reports over 20 years. 2017, this device’s year, is highlighted.

FDA decisions per year · SEL

2in 2017

2017: 2
2007high 2 (2017) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · SEL

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

Recalls per year · SEL

No recall names SEL since 2007.

Adverse event reports per year · SEL

No MAUDE report names SEL since 2007.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—00
20090—00
20100—00
20110—00
20120—00
20130—00
20140—00
20150—00
20160—00
20172—00
20180—00
20190—00
20200—00
20210—00
20220—00
20230—00
20240—00
20250—00
20260—0—

What is it indicated for?

3M™ Tegaderm™ CHG Chlorhexidine Gluconate I.V. Securement Dressing can be used to cover and protect catheter sites and to secure devices to skin. Common applications include securing and covering IV catheters, other intravascular catheters and percutaneous devices.

Tegaderm™ CHG I.V. Securement Dressing is intended to reduce vascular catheter colonization and catheter-related bloodstream infections (CRBSI) in patients with central venous or arterial catheters.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K171908: 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K171908

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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