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FDA product code KER · Class 1 · Pathology
58
Registered devices
4
Adverse events
0
Recalls
5
510(k) clearances
Devices with this code
Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYTissue-Tek® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® NanoMold™ — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® Paraform® — SAKURA FINETEK U.S.A., INC.Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYTissue-Tek® Paraform® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® Quick-Ray™ — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYTissue-Tek® Cryomold® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® Quick-Ray™ — SAKURA FINETEK U.S.A., INC.Tissue-Tek® Quick-Ray™ — SAKURA FINETEK U.S.A., INC.Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYTissue-Tek® Quick-Ray™ — SAKURA FINETEK U.S.A., INC.Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYCryomold® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.
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