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Final rule 2025-09638

Medical Devices; Clinical Chemistry and Clinical Toxicology Devices; Classification of the Plazomicin Test System

The Food and Drug Administration (FDA, Agency, or we) is classifying the plazomicin test system 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 the plazomicin test system's classification. We are taking this action because we have determined that classifying the device into class II (special controls) will provide a reasonable assurance of 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: 2026-07-31 22:49:02 UTC.

Source-supplied record

Document details

Document number
2025-09638
Published
May 29, 2025
Effective
May 29, 2025
Comments close
Not supplied
Federal Register citation
90 FR 22627

Docket identifiers

  • Docket No. FDA-2025-N-1159

CFR references

  • Title 21, part 862