LUNDY VAPORIZER SYSTEM— 510(k) K884090

Name: FDA 510(k) clearance K884090
Creator: U.S. Food and Drug Administration
Published: 1989-01-24

Substantially Equivalent

Vaporflow Technology, Inc.

FDA 510(k) clearance K884090 for LUNDY VAPORIZER SYSTEM, Substantially Equivalent on 1989-01-24. Applicant: Vaporflow Technology, Inc.. Device class: 2.

Clearance details

Applicant: Vaporflow Technology, Inc.
Product code: Code CAD
Device class: Class 2
Regulation: 21 CFR 868.5880
Advisory panel: Anesthesiology
Date received: 1988-09-28
Decision date: 1989-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code CAD

product code CAD

Malfunction: 3,275
Total: 3,275

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.