DINAMAP MPS PORTABLE MONITOR— 510(k) K971569

Substantially Equivalent

Johnson & Johnson Medical, Inc.

FDA 510(k) clearance K971569 for DINAMAP MPS PORTABLE MONITOR, Substantially Equivalent on 1997-09-19. Applicant: Johnson & Johnson Medical, Inc..

Clearance details

Applicant: Johnson & Johnson Medical, Inc.
Product code: Code MSX
Advisory panel: Cardiovascular
Date received: 1997-04-29
Decision date: 1997-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tampa, FL, US

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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.