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- 2012360233 contributor B12532818.
- 2012360233 created "c2011.".
- 2012360233 date "2011".
- 2012360233 date "c2011.".
- 2012360233 dateCopyrighted "c2011.".
- 2012360233 extent "ix, 94 p. :".
- 2012360233 identifier "9781936942145 (pbk.)".
- 2012360233 issued "2011".
- 2012360233 issued "c2011.".
- 2012360233 language "eng".
- 2012360233 publisher "Washington, DC : Thompson Pub. Group,".
- 2012360233 spatial "United States.".
- 2012360233 subject "KF3827.M4 G92 2011".
- 2012360233 subject "Medical instruments and apparatus industry Law and legislation United States.".
- 2012360233 subject "Medical technology Law and legislation United States.".
- 2012360233 subject "United States. Food and Drug Administration Rules and practice.".
- 2012360233 title "Guide to FDA's 510(k) clearance process / [editor, Max Busetti].".
- 2012360233 type "text".