PHILIPS 45 SERIES— 510(k) K933850
Substantially EquivalentPhilips Hearing Instruments Co.
FDA 510(k) clearance K933850 for PHILIPS 45 SERIES, Substantially Equivalent on 1993-09-07. Applicant: Philips Hearing Instruments Co..
Clearance details
- Applicant
- Philips Hearing Instruments Co.
- Product code
- Code ESD
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mahwah, NJ, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.