SPIROPRO— 510(k) K092324

Substantially Equivalent

Viasys Healthcare GmbH

FDA 510(k) clearance K092324 for SPIROPRO, Substantially Equivalent on 2009-09-03. Applicant: Viasys Healthcare GmbH.

Clearance details

Applicant: Viasys Healthcare GmbH
Product code: Code DQA
Advisory panel: Cardiovascular
Date received: 2009-08-04
Decision date: 2009-09-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Hoechberg, DE

Download summary PDF View on FDA.gov ↗

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.