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Cytocentrifuge
FDA product code IFB · Class 1 · Pathology
69
Registered devices
12
Adverse events
2
Recalls
3
510(k) clearances
Devices with this code
Sample Chambers w/ fast, white Cytopads, pack/48 — ELITECHGROUP INC.Thermo Fisher — SHANDON DIAGNOSTICS LIMITEDEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYCytopro® Cytocentrifuge — ELITECHGROUP INC.CELLPRESERV KOLPLAST — Kolplast C IThermo Fisher — SHANDON DIAGNOSTICS LIMITEDFisherbrand — FISHER SCIENTIFIC COMPANY L.L.C.Fisherbrand — FISHER SCIENTIFIC COMPANY L.L.C.Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYEpredia — SHANDON DIAGNOSTICS LIMITEDEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYEpredia — SHANDON DIAGNOSTICS LIMITEDThermo Fisher — SHANDON DIAGNOSTICS LIMITEDEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYEpredia — SHANDON DIAGNOSTICS LIMITEDCyto-Tek® 2500 — SAKURA FINETEK U.S.A., INC.Epredia — RICHARD-ALLAN SCIENTIFIC COMPANYThermo Fisher — SHANDON DIAGNOSTICS LIMITEDEpredia — RICHARD-ALLAN SCIENTIFIC COMPANYCytopro Cytopad, fast, white, package of 100 — ELITECHGROUP INC.Cytopro Dual Sample Chamber Caps, Pack of 48 — ELITECHGROUP INC.Fisherbrand — FISHER SCIENTIFIC COMPANY L.L.C.Epredia — SHANDON DIAGNOSTICS LIMITEDFisherbrand — FISHER SCIENTIFIC COMPANY L.L.C.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2018-06-04 | Richard-Allan Scientific Company | Mislabeled product |
| 2013-03-13 | Separation Technology, Inc. | Separation Technology, Inc. recalled SlidePrep Plus Cytology Centrifuges manufactured prior to January 1, 2013 for having the potential to start up unexpectedly |
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