PHILIP XP SERIES, IN-THE CANAL HEARING AID— 510(k) K921725
Substantially EquivalentPhilips Hearing Instruments Co.
FDA 510(k) clearance K921725 for PHILIP XP SERIES, IN-THE CANAL HEARING AID, Substantially Equivalent on 1992-08-11. Applicant: Philips Hearing Instruments Co.. Device class: 1.
Clearance details
- Applicant
- Philips Hearing Instruments Co.
- 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
- Mahwah, NJ, US
Recent devices under product code ESD
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