LIBAN INTUBATOR— 510(k) K861026

Name: FDA 510(k) clearance K861026
Creator: U.S. Food and Drug Administration
Published: 1986-07-28

Substantially Equivalent

Life Support Devices Co.

FDA 510(k) clearance K861026 for LIBAN INTUBATOR, Substantially Equivalent on 1986-07-28. Applicant: Life Support Devices Co.. Device class: 1.

Clearance details

Applicant: Life Support Devices Co.
Product code: Code CCW
Device class: Class 1
Regulation: 21 CFR 868.5540
Advisory panel: Anesthesiology
Date received: 1986-03-18
Decision date: 1986-07-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Marina Del Rey, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CCW

product code CCW

Death: 31
Injury: 136
Malfunction: 3,703
Other: 1
Total: 3,871

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.