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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K223108

TELIGEN System Navigation Ready Indications (TELIGEN Access Probe, TELIGEN Clear) · Medos International SARL · decided 2023-01-19 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
TELIGEN286202205SMedos International SàrlOLO PDQ10705034604558
(unnamed)302011012Medos International SàrlOLO10705034536156
(unnamed)302015100Medos International SàrlOLO10705034536217
(unnamed)302015020Medos International SàrlOLO10705034536187
(unnamed)302022012Medos International SàrlOLO10705034558158
(unnamed)302015030Medos International SàrlOLO10705034536200
(unnamed)302015120Medos International SàrlOLO10705034536224
TELIGEN186000002SMedos International SàrlGAD HRX LXH OLO10705034571607
(unnamed)302015025Medos International SàrlOLO10705034536194
TELIGEN186000000SMedos International SàrlGAD HRX LXH OLO PDQ10705034560359
TELIGEN286006062SMedos International SàrlOLO PDQ10705034604527