Home › Device types › KIM
Device For Sealing Microsections
FDA product code KIM · Class 1 · Pathology
72
Registered devices
10
Adverse events
1
Recalls
1
510(k) clearances
Devices with this code
Bath insert Medite/Hacker 20/40 — Leica Biosystems Nussloch GmbHBath inserts for slide racks 20, Sakura — Leica Biosystems Nussloch GmbHTissue-Tek Film® — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDTissue-Tek Film® — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDMemory 2-32 GB USB-Memory Stick — Leica Biosystems Nussloch GmbHEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDBath insert Medite/Hacker 30 — Leica Biosystems Nussloch GmbHEpredia — SHANDON DIAGNOSTICS LIMITEDTissue-Tek® Glas™ — SAKURA FINETEK U.S.A., INC.Epredia — SHANDON DIAGNOSTICS LIMITEDBath insert for slide racks Leica 20 — Leica Biosystems Nussloch GmbHOutput rack 20, pack of 6 — Leica Biosystems Nussloch GmbHEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — SHANDON DIAGNOSTICS LIMITED
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-09-04 | Leica Microsystems, Inc. | Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shoc |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsSourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.
