PHILIPS M60 SERIES— 510(k) K920142
Substantially EquivalentPhilips Int'L B.V.
FDA 510(k) clearance K920142 for PHILIPS M60 SERIES, Substantially Equivalent on 1992-01-23. Applicant: Philips Int'L B.V.. Device class: 1.
Clearance details
- Applicant
- Philips Int'L B.V.
- 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
view allMore clearances from Philips Int'L B.V.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.