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The Food and Drug Administration (FDA, the Agency, or we) is classifying the laparoscopic gastrointestinal sizing tool 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 classification of the laparoscopic gastrointestinal sizing tool. We are taking this action because we have determined that classifying the device into class II 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.
Published
Aug 21, 2025
Effective
Aug 21, 2025
Citation
90 FR 40728
Agencies
2
Full text not available in our database.
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Docket No. FDA-2025-N-2823
21 CFR 876