SPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology— 510(k) K241953
Substantially EquivalentPAJUNK GmbH Medizintechnologie
FDA 510(k) clearance K241953 for SPROTTE® STANDARD (LUER/ NRFit®) Anesthesiology, Substantially Equivalent on 2024-11-22. Applicant: PAJUNK GmbH Medizintechnologie.
Clearance details
- Applicant
- PAJUNK GmbH Medizintechnologie
- Product code
- Code BSP
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Geisingen, DE
Adverse events under product code BSP
product code BSP- Death
- 2
- Total
- 2
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.