PHILIPS 41 SERIES RAINBOW— 510(k) K920134
Substantially EquivalentPhilips Int'L B.V.
FDA 510(k) clearance K920134 for PHILIPS 41 SERIES RAINBOW, Substantially Equivalent on 1992-01-24. 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
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