FUKUDA DENSHI DYNASCOPE MODEL DS-7141 PORTABLE PATIENT MONITOR— 510(k) K040246

Name: FDA 510(k) clearance K040246
Creator: U.S. Food and Drug Administration
Published: 2004-05-26

Substantially Equivalent

Fukuda Denshi USA, Inc.

FDA 510(k) clearance K040246 for FUKUDA DENSHI DYNASCOPE MODEL DS-7141 PORTABLE PATIENT MONITOR, Substantially Equivalent on 2004-05-26. Applicant: Fukuda Denshi USA, Inc.. Device class: 2.

Clearance details

Applicant: Fukuda Denshi USA, Inc.
Product code: Code MHX
Device class: Class 2
Regulation: 21 CFR 870.1025
Advisory panel: Cardiovascular
Date received: 2004-02-03
Decision date: 2004-05-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Redmond, WA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MHX

product code MHX

Death: 580
Injury: 2,441
Malfunction: 12,655
Other: 3
Total: 15,679

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.