REXTON RX12PP, RX20PP & RX34PP IN-THE-EAR HEAR AID— 510(k) K892333
Substantially EquivalentRexton, Inc.
FDA 510(k) clearance K892333 for REXTON RX12PP, RX20PP & RX34PP IN-THE-EAR HEAR AID, Substantially Equivalent on 1989-05-19. Applicant: Rexton, Inc..
Clearance details
- Applicant
- Rexton, Inc.
- Product code
- Code ESD
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, MN, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.