Obstetrical & Gynecological 10
- Testing of Tissue Containment Systems Used During Power Morcellation Procedures
- Mouse Embryo Assay Testing for Assisted Reproduction Technology Devices
- Product Labeling Requirements for Laparoscopic Power Morcellators in Gynecologic Surgery
- 510k Exemption for Unclassified Medical Devices in Selected Product Categories
- Labeling Requirements for Ultrasonic Surgical Aspirator Devices - Contraindication for Uterine Fibroid Procedures
- Evaluation and Reporting of Age, Race, and Ethnicity Data in Medical Device Clinical Studies
- Procedures for Medical Devices Advisory Committee Panel Meetings
- Use of Real-World Data to Generate Evidence for Medical Device Regulatory Decisions
- Assessment of Radiofrequency-Induced Heating in Multi-Configuration Passive Medical Devices for MR Conditional Labeling
- Applying Human Factors Engineering and Usability Engineering to Medical Devices