RETROX— 510(k) DEN020003
UnknownAuric Hearing Systems, Inc.
FDA 510(k) clearance DEN020003 for RETROX, Unknown on 2002-08-20. Applicant: Auric Hearing Systems, Inc..
Clearance details
- Applicant
- Auric Hearing Systems, Inc.
- Product code
- Code NIX
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Post-NSE
- Location
- Nahant, MA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.