MEDO BUBBLE BATH MA-80, 400, 600 & 700— 510(k) K844064

Name: FDA 510(k) clearance K844064
Creator: U.S. Food and Drug Administration
Published: 1985-01-23

Substantially Equivalent

Medo U.S.A., Inc.

FDA 510(k) clearance K844064 for MEDO BUBBLE BATH MA-80, 400, 600 & 700, Substantially Equivalent on 1985-01-23. Applicant: Medo U.S.A., Inc.. Device class: 2.

Clearance details

Applicant: Medo U.S.A., Inc.
Product code: Code ILJ
Device class: Class 2
Regulation: 21 CFR 890.5100
Advisory panel: Physical Medicine
Date received: 1984-10-18
Decision date: 1985-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wood Dale, IL, US

Download summary PDF View on FDA.gov ↗

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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.