INTEGRATED PATIENT MONITORING SYSTEM— 510(k) K041918

Substantially Equivalent

Invivo Research, Inc.

FDA 510(k) clearance K041918 for INTEGRATED PATIENT MONITORING SYSTEM, Substantially Equivalent on 2004-10-15. Applicant: Invivo Research, Inc..

Clearance details

Applicant: Invivo Research, Inc.
Product code: Code MWI
Advisory panel: Cardiovascular
Date received: 2004-07-16
Decision date: 2004-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orlando, FL, US

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Adverse events under product code MWI

product code MWI

Death: 16
Malfunction: 963
Total: 979

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.