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Microtome, Rotary
FDA product code IDO · Class 1 · Pathology
36
Registered devices
56
Adverse events
1
Recalls
5
510(k) clearances
Devices with this code
Clarapath™ SectionStar™ — Clarapath, Inc.Epredia — SHANDON DIAGNOSTICS LIMITEDMT1 Rotary Microtome — Dakewe (Shenzhen) Medical Equipment Co., Ltd.Epredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDTissue-Tek® — SAKURA FINETEK U.S.A., INC.Accu-Cut® SRM™ 300 LT — SAKURA FINETEK U.S.A., INC.Accu-Cut® SRM™ 200 — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDAccu-Cut® SRM™ 200 — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDAccu-Cut® SRM™ 300 LT — SAKURA FINETEK U.S.A., INC.Tissue-Tek AutoSection® — SAKURA FINETEK U.S.A., INC.Tissue-Tek® — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITED2065A Auto Microtome — Dakewe (Shenzhen) Medical Equipment Co., Ltd.Epredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDAccu-Cut® SRM™ 200 — SAKURA FINETEK U.S.A., INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2011-08-12 | Richard-Allan Scientific Company | The firm has received two complaints of finger lacerations in operators of this device. |
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