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Home » DOL:Federal Contract Compliance Programs Office

DOL:Federal Contract Compliance Programs Office

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  • Construction and Urban-Development benchmark logo

    Benchmark: Rescission of Executive Order 11246: Federal Contracting Compliance Requirements

  • Icon showing a crane amongst skyscrapers

    Rescission of Executive Order 11246: Federal Contracting Compliance Requirements

    $129.99
  • Healthcare benchmark logo

    Benchmark: Section 503 Regulatory Changes: Compliance for Federal Contractors

  • an icon representing Public Health

    Section 503 Regulatory Changes: Compliance for Federal Contractors

    $129.99
  • an icon representing Public Health

    VEVRAA Regulatory Update: Compliance Changes for Federal Contractors

    $49.99
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    • Construction and Urban Development
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  • Publication Year
    • 2026
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DOL:Federal Contract Compliance Programs Office

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FDA Regulation: Focused Ultrasound Systems for Non-Thermal, Mechanical Tissue Ablation

Oct 7, 2026

Why This Course is Important
Without this course, you risk overlooking critical compliance steps, potentially leading to market denial, enforcement actions, and increased legal or financial exposure for your organization.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; General and Plastic Surgery Devices; Classification of the Focused Ultrasound System for Non-Thermal, Mechanical Tissue Ablation.

Key regulatory references include:

  • 21 CFR Part 878 – General and Plastic Surgery Devices

Course SKU
FR-26-2252-1

FDA Rule: Class II Classification for Hyperoxia Monitoring Device Adjunct to Pulse Oximetry

Oct 7, 2026

Why This Course is Important
Without this course, you risk missing critical compliance deadlines, misunderstanding special control requirements, and facing potential enforcement actions that could delay or block your product’s entry to market.

Course Details
This is a self-paced eLearning course based on the Federal Register Document titled Medical Devices; Cardiovascular Devices; Classification of the Hyperoxia Monitoring Device Adjunct to Pulse Oximetry.

Key regulatory references include:

  • 21 CFR Part 870 – Cardiovascular Devices

Course SKU
FR-26-2251-1

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