STASILON FR— 510(k) K072890

Substantially Equivalent

Entegrion, Inc.

FDA 510(k) clearance K072890 for STASILON FR, Substantially Equivalent on 2007-12-10. Applicant: Entegrion, Inc..

Clearance details

Applicant: Entegrion, Inc.
Product code: Code QSY
Advisory panel: Unknown
Date received: 2007-10-10
Decision date: 2007-12-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Research Triangle Park, NC, US

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Adverse events under product code QSY

product code QSY

Death: 5
Other: 1
Total: 6

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.