MBATH 1000 (60)— 510(k) K052479

Name: FDA 510(k) clearance K052479
Creator: U.S. Food and Drug Administration
Published: 2006-01-26

Substantially Equivalent

Enneking Medical, Inc.

FDA 510(k) clearance K052479 for MBATH 1000 (60), Substantially Equivalent on 2006-01-26. Applicant: Enneking Medical, Inc.. Device class: 2.

Clearance details

Applicant: Enneking Medical, Inc.
Product code: Code ILJ
Device class: Class 2
Regulation: 21 CFR 890.5100
Advisory panel: Physical Medicine
Date received: 2005-09-09
Decision date: 2006-01-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kansas City, MO, US

Download summary PDF View on FDA.gov ↗

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K012057 — CASCADE BATH, MODEL 69002001-07-19
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Adverse events under product code ILJ

product code ILJ

Death: 4
Total: 4

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.