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

Clearance record K193548

Mirage Hydrophilic Guidewire, X-pedion Hydrophilic Guidewire · Micro Therapeutics, Inc. d/b/a ev3 Neurovascular · decided 2020-01-18 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Mirage103-0608Micro Therapeutics, Inc.DQX MOF00763000294120
X-Pedion103-0605-200Micro Therapeutics, Inc.DQX MOF00763000518929
Mirage103-0608Micro Therapeutics, Inc.DQX MOF00763000518912
X-Pedion103-0605-200Micro Therapeutics, Inc.DQX MOF00763000294113