HEALTHLINE REDI-NEB MEDICATION NEBULIZER, MODEL RN-510— 510(k) K080969

Name: FDA 510(k) clearance K080969
Creator: U.S. Food and Drug Administration
Published: 2008-07-25

Substantially Equivalent

Medi Nuclear Corp., Inc.

FDA 510(k) clearance K080969 for HEALTHLINE REDI-NEB MEDICATION NEBULIZER, MODEL RN-510, Substantially Equivalent on 2008-07-25. Applicant: Medi Nuclear Corp., Inc.. Device class: 2.

Clearance details

Applicant: Medi Nuclear Corp., Inc.
Product code: Code CAF
Device class: Class 2
Regulation: 21 CFR 868.5630
Advisory panel: Anesthesiology
Date received: 2008-04-04
Decision date: 2008-07-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Baldwin Park, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAF

product code CAF

Death: 22
Injury: 125
Malfunction: 613
Other: 11
Total: 771

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.