THROAT MOI-STIR— 510(k) K840807

Name: FDA 510(k) clearance K840807
Creator: U.S. Food and Drug Administration
Published: 1984-05-25

Substantially Equivalent

Kingswood Laboratories, Inc.

FDA 510(k) clearance K840807 for THROAT MOI-STIR, Substantially Equivalent on 1984-05-25. Applicant: Kingswood Laboratories, Inc.. Device class: Unclassified.

Clearance details

Applicant: Kingswood Laboratories, Inc.
Product code: Code LFD
Device class: Unclassified
Advisory panel: Unknown
Date received: 1984-02-24
Decision date: 1984-05-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LFD

product code LFD

Death: 3
Total: 3

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.