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FDA Proposed Reclassification: Cystoscopic Systems for Bladder Cancer Detection

Aug 17, 2026

Why This Course is Important
Without this course, you may overlook critical compliance updates, risk misinterpreting regulatory requirements, or miss new opportunities for device innovation and patient access in bladder cancer detection.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Gastroenterology-Urology Devices; Reclassification of Diagnostic Endoscopic Light Source Systems To Be Renamed Cystoscopic Systems Intended as an Aid for Detection of Bladder Cancer.

Key regulatory references include:

Course SKU
FR-26-2153-1

FDA Proposed Rule: Class I Classification for Distinct Medical Device Accessories

Aug 17, 2026

Why This Course is Important
Missing this course could result in overlooked opportunities for regulatory streamlining, non-compliance risks, and missed chances to influence FDA policy affecting accessory classification.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Classification of Accessories Distinct From Other Devices; Proposed List of Accessories Suitable for Class I; Request for Comments.

Key regulatory references include:

Course SKU
FR-26-2152-1

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