Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
3
|
| pubmed:dateCreated |
1997-9-4
|
| pubmed:abstractText |
The Food and Drug Administration's (FDA) checkout recommendations are to be applied, at least daily, on anesthesia machines. Devices included in the checkout are crucial to the safe operation of the machine. Remaining devices do not need to be checked as often. However, they should be checked at some appropriate interval. We calculated the reliability of the non-FDA checkout devices, to predict failure rates of these devices.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
May
|
| pubmed:issn |
0748-1977
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
13
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
171-9
|
| pubmed:dateRevised |
2004-11-17
|
| pubmed:meshHeading | |
| pubmed:year |
1997
|
| pubmed:articleTitle |
Performance of anesthesia machines' devices that are not part of the Food and Drug Administration's daily checkout.
|
| pubmed:affiliation |
Department of Anesthesia, University of Iowa, Iowa City 52242, USA. franklin-dexter@-uiowa.edu
|
| pubmed:publicationType |
Journal Article
|