TINNITUS SOUND GENERATOR MODULE— 510(k) K110932
Substantially EquivalentGn Resound A/S
FDA 510(k) clearance K110932 for TINNITUS SOUND GENERATOR MODULE, Substantially Equivalent on 2011-05-03. Applicant: Gn Resound A/S.
Clearance details
- Applicant
- Gn Resound A/S
- Product code
- Code KLW
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Ballerup, DK
Data sourced from openFDA. This site is unofficial and independent of the FDA.