STIMUPLEX PEN— 510(k) K061983

Substantially Equivalent

Stockert GmbH

FDA 510(k) clearance K061983 for STIMUPLEX PEN, Substantially Equivalent on 2006-11-21. Applicant: Stockert GmbH.

Clearance details

Applicant: Stockert GmbH
Product code: Code BXN
Advisory panel: Anesthesiology
Date received: 2006-07-13
Decision date: 2006-11-21
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Freiburg, B-W, DE

Download summary PDF View on FDA.gov ↗

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.