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.. Device class: 1.
Clearance details
- Applicant
- Rexton, Inc.
- Product code
- Code ESD
- Device class
- Class 1
- Regulation
- 21 CFR 874.3300
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Plymouth, MN, US
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