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Final rule 2026-18432

Medical Devices; Cardiovascular Devices; Classification of the Temperature Regulation Device for Esophageal Protection During Cardiac Ablation Procedures

The Food and Drug Administration (FDA) is classifying the temperature regulation device for esophageal protection during cardiac ablation procedures 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 temperature regulation device for esophageal protection during cardiac ablation procedures. 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: 2026-09-10 22:49:02 UTC.

Source-supplied record

Document details

Document number
2026-18432
Published
Sep 10, 2026
Effective
Sep 10, 2026
Comments close
Not supplied
Federal Register citation
91 FR 57500

Docket identifiers

  • Docket No. FDA-2026-N-9910

CFR references

  • Title 21, part 870