510(k) · Cleared
ClearedVichy Shower
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bouvier Hydro, Inc. · ILJ Bath, Hydro-Massage
Cleared on Aug 11, 1998 after a 154-day review. FDA’s file for it is a 510(k) statement, which names no predicate.
- Decided
- Aug 11, 1998
- Review
- 154 days
- Class
- Class II
- Product code
- ILJ
- Recalls
- None
- Predicates
- 0
FDA’s file for it is a 510(k) statement, which names no predicate.
Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in ILJ? 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
What was it cleared against?
FDA’s file for it is a 510(k) statement, which names no predicate.
What descends from it?
No later submission names this one as a predicate yet.
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.
How does its category compare?
All ILJ devicesILJ Bath, Hydro-Massage: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · ILJ
1in 2011
2026 to Oct 25, outlined.
Median 510(k) review, days · ILJ
Too few ILJ 510(k)s in any year since 2007 to give a median.
Recalls per year · ILJ
No recall names ILJ since 2007.
Adverse event reports per year · ILJ
11in 2025
MAUDE reports naming product code ILJ, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 14 |
| 2008 | 0 | — | 0 | 7 |
| 2009 | 1 | — | 0 | 22 |
| 2010 | 0 | — | 0 | 10 |
| 2011 | 1 | — | 0 | 12 |
| 2012 | 0 | — | 0 | 85 |
| 2013 | 0 | — | 0 | 210 |
| 2014 | 0 | — | 0 | 188 |
| 2015 | 0 | — | 0 | 72 |
| 2016 | 0 | — | 0 | 57 |
| 2017 | 0 | — | 0 | 26 |
| 2018 | 0 | — | 0 | 21 |
| 2019 | 0 | — | 0 | 22 |
| 2020 | 0 | — | 0 | 14 |
| 2021 | 0 | — | 0 | 6 |
| 2022 | 0 | — | 0 | 12 |
| 2023 | 0 | — | 0 | 13 |
| 2024 | 0 | — | 0 | 11 |
| 2025 | 0 | — | 0 | 11 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
Vichy Shower is used in hydrotherapy to relieve pain and itching and as an aid in the removal of contaminated tissue, and in the healing process of inflamed and traumatized tissue.
Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K980909 · printed Nov 6, 2026
Cite this page
510(k) Report. “K980909: Vichy Shower.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K980909
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026