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

Clearance record K111254

RELIEVA SOLO ELITE SINUS BALLOON CATHETER · Acclarent, Inc. · decided 2011-08-22 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
RELIEVA ULTIRRABC0516RUACCLARENT, INC.LRC10705031200258
RELIEVA ULTIRRABC0724RUACCLARENT, INC.LRC10705031200296
RELIEVA ULTIRRABC0716RUACCLARENT, INC.LRC10705031200289
RELIEVA ULTIRRABC0616RUACCLARENT, INC.LRC10705031200272