共 50 条
- [21] USES OF TOXICOLOGY DATA FOR MEDICAL DEVICES - THE FDA PERSPECTIVE [J]. JOURNAL OF THE AMERICAN COLLEGE OF TOXICOLOGY, 1988, 7 (04): : 499 - 507
- [22] FDA recognizes: Simulation essential to evaluate medical devices [J]. Adv Mater Processes, 4 (32-33):
- [23] Tort law deference to FDA regulation of medical devices [J]. GEORGETOWN LAW JOURNAL, 2000, 88 (07) : 2119 - 2145
- [24] SUBSTANTIALLY UNEQUIVALENT: REFORMING FDA REGULATION OF MEDICAL DEVICES [J]. UNIVERSITY OF ILLINOIS LAW REVIEW, 2014, (04): : 1363 - 1400
- [26] FDA Recognizes Simulation Essential to Evaluate Medical Devices [J]. ADVANCED MATERIALS & PROCESSES, 2013, 171 (04): : 32 - 33
- [27] What does "FDA Approved" mean for medical devices? [J]. OBSTETRICS AND GYNECOLOGY, 2008, 111 (01): : 4 - 6
- [29] Combining FDA labeling and LLDP for securing networked medical devices [J]. Biomedical Instrumentation and Technology, 2016, 50 : 48 - 51
- [30] Industry perspective on FDA regulation of medical devices and the practice of medicine [J]. ANNALS OF THORACIC SURGERY, 1996, 61 (01): : 485 - 486