OXYGEN MONITOR 140/141— 510(k) K812040

Substantially Equivalent

Medix Medical Electronics (U.S.A.), Inc.

FDA 510(k) clearance K812040 for OXYGEN MONITOR 140/141, Substantially Equivalent on 1981-09-21. Applicant: Medix Medical Electronics (U.S.A.), Inc..

Clearance details

Applicant: Medix Medical Electronics (U.S.A.), Inc.
Product code: Code CCL
Advisory panel: Anesthesiology
Date received: 1981-07-21
Decision date: 1981-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code CCL

product code CCL

Other: 2
Total: 2

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.