TELIGEN System Peripheral Motor Nerve Stimulation Indications— 510(k) K223438
Substantially EquivalentMedos International SARL
FDA 510(k) clearance K223438 for TELIGEN System Peripheral Motor Nerve Stimulation Indications, Substantially Equivalent on 2023-02-10. Applicant: Medos International SARL. Device class: 2.
Clearance details
- Applicant
- Medos International SARL
- Product code
- Code PDQ
- Device class
- Class 2
- Regulation
- 21 CFR 874.1820
- Advisory panel
- Ear, Nose, Throat
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Le Locle, CH
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