LINK TO ACUITY CLINICIAN NOTIFIER— 510(k) K070204

Name: FDA 510(k) clearance K070204
Creator: U.S. Food and Drug Administration
Published: 2007-03-23

Substantially Equivalent

Welch Allyn Protocol, Inc.

FDA 510(k) clearance K070204 for LINK TO ACUITY CLINICIAN NOTIFIER, Substantially Equivalent on 2007-03-23. Applicant: Welch Allyn Protocol, Inc.. Device class: 2.

Clearance details

Applicant: Welch Allyn Protocol, Inc.
Product code: Code MSX
Device class: Class 2
Regulation: 21 CFR 870.2300
Advisory panel: Cardiovascular
Date received: 2007-01-22
Decision date: 2007-03-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Beaverton, OR, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MSX

product code MSX

Death: 59
Total: 59

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.