PERIFORM PERINEOMETRIC PROBE, MODEL 8300— 510(k) K002617
Substantially EquivalentNeen Design , Ltd.
FDA 510(k) clearance K002617 for PERIFORM PERINEOMETRIC PROBE, MODEL 8300, Substantially Equivalent on 2001-04-05. Applicant: Neen Design , Ltd..
Clearance details
- Applicant
- Neen Design , Ltd.
- Product code
- Code HIR
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dereham, Norfolk, GB
Data sourced from openFDA. This site is unofficial and independent of the FDA.