MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098— 510(k) K070134
Substantially EquivalentStockert GmbH
FDA 510(k) clearance K070134 for MODIFICATION TO STIMUPLEX HNS-12, MODEL 4892098, Substantially Equivalent on 2007-03-22. Applicant: Stockert GmbH.
Clearance details
- Applicant
- Stockert GmbH
- Product code
- Code BXN
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Freiburg, B-W, DE
Adverse events under product code BXN
product code BXN- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . 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.