SATURATION/HEMATOCRIT MONITOR SYSTEM— 510(k) K910421

Substantially Equivalent

Medtronic Vascular

FDA 510(k) clearance K910421 for SATURATION/HEMATOCRIT MONITOR SYSTEM, Substantially Equivalent on 1991-10-15. Applicant: Medtronic Vascular.

Clearance details

Applicant: Medtronic Vascular
Product code: Code DRY
Advisory panel: Cardiovascular
Date received: 1991-01-30
Decision date: 1991-10-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Anaheim, CA, US

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Adverse events under product code DRY

product code DRY

Death: 5
Total: 5

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.