510(k) Report

510(k) · Cleared

Cleared

Water Treatment System for Hemodialysis

K983512510(k) TraditionalCleared Apr 28, 1999203-day reviewClass II21 CFR 876.5665

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

Water Vault, Inc. · FIP Subsystem, Water Purification

Cleared on Apr 28, 1999 as substantially equivalent to K945559 (Mar Cor Services, Inc., 1996) after a 203-day review. Its family tree reaches back 2 generations to 1987.

Decided
Apr 28, 1999
Review
203 days
Class
Class II
Product code
FIP
Recalls
None
Predicates
1

Its longest line of descent runs back 2 generations to K873487 (1987). 3 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 2 generations backK873487 HD-400-a/B/C Hemodialysis Systems & AccessoriesWater Pure, Inc. · 1987
  2. 1 generation backK945559 Mar Cor Complete Water Treatment System for Kdney DialysisMar Cor Services, Inc. · 1996
  3. This deviceK983512 Water Treatment System for HemodialysisWater Vault, Inc. · 1999
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−2K873487HD-400-a/B/C Hemodialysis Systems & AccessoriesWater Pure, Inc.1987—
−1K945559Mar Cor Complete Water Treatment System for Kdney DialysisMar Cor Services, Inc.1996—
0 (this device)K983512Water Treatment System for HemodialysisWater Vault, Inc.1999—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198910
FIG. 1 — Lineage of K983512, 1987–1999Source: 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 FIP? 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 FIP device

  1. #1 K251851 DIASAFEplusUS (F00013010)score 14.1 · 14 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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What was it cleared against? (1)

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
*K945559Mar Cor Complete Water Treatment System for Kdney Dialysis
Summary page 1
…for Hemodialysis Class II Device Legally Marketed Predicate Device - MARCOR Water Treatment System For Hemodialysis K#945559 Predicate Device Water Vault Inc. MARCOR #K945559 INTENDED UsE Hemodialysis Hemodialysis EQUIPMENT: Makes Use Of Existing FDA Makes Use Of Existing FDA Cleared Reverse Osmosis U…
Mar Cor Services, Inc.1996—

Also cleared against K945559: 3 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)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • The line of descent spans 12 years and passes through 3 companies; a new generation was cleared every 8.6 years on median.
  • None of the 3 ancestors has a recall.
  • 3 other devices also cite its predicate K945559.

How does its category compare?

All FIP devices

FIP Subsystem, Water Purification: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · FIP

4in 2025

2007: 12008: 32009: 32010: 22011: 42012: 22013: 42014: 42015: 22016: 22017: 12018: 12019: 22020: 12021: 12022: 12023: 32024: 12025: 4
2007high 4 (2011) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FIP

88in 2025

2008: 202 days median2009: 167 days median2011: 116 days median2013: 125 days median2014: 126 days median2023: 69 days median2025: 88 days median
2007high 202 (2008) · low 69 (2023)2026

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

Recalls per year · FIP

1in 2020

2020: 1
2007high 1 (2020) · low 0 (2007)2026

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

Adverse event reports per year · FIP

77in 2025

2007: 12008: 52010: 122011: 42012: 42013: 412014: 342015: 122016: 32017: 62018: 32019: 132020: 122021: 352022: 572023: 1402024: 1742025: 77
2007high 174 (2024) · low 0 (2009)2025

MAUDE reports naming product code FIP, 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—01
2008320205
2009316700
20102—012
2011411604
20122—04
20134125041
20144126034
20152—012
20162—03
20171—06
20181—03
20192—013
20201—112
20211—035
20221—057
20233690140
20241—0174
2025488077
20260—0—

What is it indicated for?

The WaterVault Cube Water Treatment System for HemoDialysis is intended to remove organic and inorganic substances and microbial contaminants from water used to dilute dialysate concentrate to form dialysate.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K983512: Water Treatment System for Hemodialysis.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K983512

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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