FDA 510(k) Applications Submitted by Matthias Kollek

FDA 510(k) Number Submission Date Device Name Applicant
K240932 04/05/2024 HybridTherm System Erbe Elektromedizin GmbH
K231023 04/11/2023 ERBEJET« 2 System Erbe Elektromedizin GmbH
K232033 07/07/2023 HYBRIDknife« flex Erbe Elektromedizin GmbH
K242044 07/12/2024 FiAPC plus probes Erbe Elektromedizin GmbH
K243120 09/30/2024 HybridAPC probe Erbe Elektromedizin GmbH
K243451 11/07/2024 FiAPC plus probes Erbe Elektromedizin GmbH


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