| Record ID | marc_loc_2016/BooksAll.2016.part23.utf8:202350642:1261 |
| Source | Library of Congress |
| Download Link | /show-records/marc_loc_2016/BooksAll.2016.part23.utf8:202350642:1261?format=raw |
LEADER: 01261nam a2200241 a 4500
001 94151659
003 DLC
005 19950724164528.4
008 940428s1993 dcua b 100 0 eng
010 $a 94151659
040 $aDLC$cDLC
050 00 $aR856.6$b.H55 1992
082 00 $a681/.761/028553$220
111 2 $aHIMA Conference$d(1992 :$cWashington, D.C.)
245 10 $aMedical device software development and product submissions :$bproceedings of the 1992 HIMA Conference /$csponsored by the Health Industry Manufacturers Association, Washington, D.C., December 1-2, 1992.
260 $aWashington, D.C. (1200 G St., N.W., Suite 400, Washington 20005) :$bThe Association,$cc1993.
300 $a172, 6, 40 p. :$bill. ;$c28 cm.
440 0 $aHIMA publication ;$v93-5
500 $aIncludes Appendix B: Reviewer guidance for computer controlled medical devices undergoing 510(k) review / Office of Device Evaluation, Center for Devices and Radiological Health, Food and Drug Administration.
504 $aIncludes bibliographical references.
650 0 $aMedical instruments and apparatus$xSoftware$xCongresses.
710 20 $aHealth Industry Manufacturers Association.
740 01 $aReviewer guidance for computer controlled medical devices undergoing 510(k) review.