VITALMAX 830 SERIES— 510(k) K913263

Substantially Equivalent

Pace Tech, Inc.

FDA 510(k) clearance K913263 for VITALMAX 830 SERIES, Substantially Equivalent on 1991-10-10. Applicant: Pace Tech, Inc..

Clearance details

Applicant: Pace Tech, Inc.
Product code: Code MHX
Advisory panel: Cardiovascular
Date received: 1991-07-23
Decision date: 1991-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clearwater, FL, US

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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.