FLOWLOCK OXYGEN METER— 510(k) K811162

Name: FDA 510(k) clearance K811162
Creator: U.S. Food and Drug Administration
Published: 1981-05-08

Substantially Equivalent

Lifeguard Medical Products, Inc.

FDA 510(k) clearance K811162 for FLOWLOCK OXYGEN METER, Substantially Equivalent on 1981-05-08. Applicant: Lifeguard Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Lifeguard Medical Products, Inc.
Product code: Code BYJ
Device class: Class 2
Regulation: 21 CFR 868.5655
Advisory panel: Anesthesiology
Date received: 1981-04-28
Decision date: 1981-05-08
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 BYJ

product code BYJ

Death: 16
Total: 16

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.