|
|
Volumn 40, Issue 2, 2004, Pages 395-396
|
|
Medical device adverse event reports and the Food and Drug Administration
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
CAUTERIZATION;
DEVICE;
EDITORIAL;
FOOD AND DRUG ADMINISTRATION;
HEALTH CARE POLICY;
HUMAN;
IATROGENIC DISEASE;
MEDICAL DECISION MAKING;
MEDICAL ETHICS;
MEDICAL INSTRUMENTATION;
PATIENT CARE;
PRIORITY JOURNAL;
SAFETY;
VASCULAR SURGERY;
ETHICS;
MANDATORY REPORTING;
POSTMARKETING SURVEILLANCE;
UNITED STATES;
DEVICE APPROVAL;
ETHICS, MEDICAL;
HUMANS;
MANDATORY REPORTING;
PRODUCT SURVEILLANCE, POSTMARKETING;
UNITED STATES;
|
|
EID: 3442899311
PISSN: 07415214
EISSN: None
Source Type: Journal
DOI: 10.1016/j.jvs.2004.04.030 Document Type: Editorial |
|
Times cited : (1)
|
|
References (0)
|
