VITALMAX 510/520— 510(k) K912880

Substantially Equivalent

Pace Tech, Inc.

FDA 510(k) clearance K912880 for VITALMAX 510/520, Substantially Equivalent on 1991-11-14. Applicant: Pace Tech, Inc..

Clearance details

Applicant: Pace Tech, Inc.
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 1991-07-01
Decision date: 1991-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

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Adverse events under product code DQA

product code DQA

Death: 66
Malfunction: 2,867
Other: 1
Total: 2,934

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.