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RI-MINI — Rudolf Riester GmbH & Co. KG (510(k) K932503)

RI-MINI — Rudolf Riester GmbH & Co. KG (510(k) K932503) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: RI-MINI; Applicant: Rudolf Riester GmbH & Co. KG; Clearance track: 510(k).

Device nameRI-MINI
ApplicantRudolf Riester GmbH & Co. KG
Clearance track510(k)
Submission numberK932503
DecisionSubstantially Equivalent
Decision date1993-10-08
Date received1993-05-21
Product codeERA
Device class1
Medical specialtyEar, Nose, Throat
Applicant locationDE
SourceopenFDA device

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