TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear)— 510(k) K223108
Substantially EquivalentMedos International SARL
FDA 510(k) clearance K223108 for TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear), Substantially Equivalent on 2023-01-19. Applicant: Medos International SARL. Device class: 2.
Clearance details
- Applicant
- Medos International SARL
- Product code
- Code OLO
- Device class
- Class 2
- Regulation
- 21 CFR 882.4560
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lelocle, CH
Recent devices under product code OLO
view allMore clearances from Medos International SARL
view allAdverse events under product code OLO
product code OLO- Death
- 11
- Injury
- 2,799
- Malfunction
- 11,105
- Other
- 1
- Total
- 13,916
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.