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Ki Mobility, LLC

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories3
Latest FDA decision2023-09-05
TypeNumberDevice NameCodeDateActions
510(k) K200583 Ki Mobility Focus CR, Ki Mobility Focus CRe, Ki Mobility Focus CR TTLIOR2023-09-05 View
510(k) K201869 Ki Power Tilt SystemITI2023-09-05 View
510(k) K223533 Little Wave Arc; Little Wave FlipLBE2023-08-31 View
510(k) K223527 Little Wave Clik, Rogue XP, Little Wave XP, SparkIOR2023-08-31 View
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