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Final rule 2026-20725

Medical Devices; Immunology and Microbiology Devices; Classification of the Hematopoietic Cell Enrichment Kit

The Food and Drug Administration (FDA) is classifying the hematopoietic cell enrichment kit into class II (special controls). The special controls that apply to the device type are identified in this order and will be part of the codified language for classification of the hematopoietic cell enrichment kit. We are taking this action because we have determined that classifying the device into class II will provide a reasonable assurance of the safety and effectiveness of the device. We believe this action will also enhance patients' access to beneficial innovative devices, in part by reducing regulatory burdens.

Source: FederalRegister.gov API v1Recently refreshed. Last successful refresh: 2026-10-09 08:49:02 UTC.

Source-supplied record

Document details

Document number
2026-20725
Published
Oct 9, 2026
Effective
Oct 9, 2026
Comments close
Not supplied
Federal Register citation
91 FR 64609

Docket identifiers

  • Docket No. FDA-2026-N-10994

CFR references

  • Title 21, part 866