MULTISTIM— 510(k) K011308

Substantially Equivalent

Pajunk GmbH

FDA 510(k) clearance K011308 for MULTISTIM, Substantially Equivalent on 2001-11-29. Applicant: Pajunk GmbH.

Clearance details

Applicant: Pajunk GmbH
Product code: Code BXN
Advisory panel: Anesthesiology
Date received: 2001-04-30
Decision date: 2001-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flemington, NJ, US

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Adverse events under product code BXN

product code BXN

Other: 1
Total: 1

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.