CARDIOPULMONARY EXERCISE TESTING OPTION TO INNOCOR— 510(k) K071911

Substantially Equivalent

Innovision A/S

FDA 510(k) clearance K071911 for CARDIOPULMONARY EXERCISE TESTING OPTION TO INNOCOR, Substantially Equivalent on 2007-09-07. Applicant: Innovision A/S.

Clearance details

Applicant: Innovision A/S
Product code: Code DQK
Advisory panel: Cardiovascular
Date received: 2007-07-11
Decision date: 2007-09-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Lake Forest, IL, US

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Adverse events under product code DQK

product code DQK

Death: 10
Injury: 225
Malfunction: 2,123
Other: 2
Total: 2,360

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.