Medical Device Manufacturing and Medical Device Reports (MDR)
Insight
.
2009 Jul-Sep;34(3):24-5.
Author
Veronica Arellano
1
Affiliation
1
veronica.arellano@alconlabs.com
PMID:
19708431
No abstract available
MeSH terms
Device Approval*
Equipment and Supplies / standards*
Humans
Product Surveillance, Postmarketing / methods*
Registries*
United States
United States Food and Drug Administration