PAJUNK INFILTRALONG WOUND INFILTRATION CATHETER KIT— 510(k) K080675
Substantially EquivalentPAJUNK GmbH Medizintechnologie
FDA 510(k) clearance K080675 for PAJUNK INFILTRALONG WOUND INFILTRATION CATHETER KIT, Substantially Equivalent on 2008-06-20. Applicant: PAJUNK GmbH Medizintechnologie.
Clearance details
- Applicant
- PAJUNK GmbH Medizintechnologie
- Product code
- Code BSO
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Geisingen, DE
Adverse events under product code BSO
product code BSO- Malfunction
- 688
- Total
- 688
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.