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Title FDA and industry actions on premarket notification (510(k)) submissions, effect on FDA review clock and performance assessment [electronic resource].

Imprint Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health : Center for Biologics Evaluation and Research, [2004]

Copies

Location Call No. OPAC Message Status
 Axe Federal Documents Online  HE 20.4802:F 73/2    ---  Available
Description 14 p. : digital, PDF file
System Details Mode of access via the FDA CBER web site.
Note Title from PDF title page (viewed on May 22, 2009).
"Document issued on: May 21, 2004".
Subject User charges -- United States.
Medical instruments and apparatus -- United States -- Evaluation.
Added Author Center for Devices and Radiological Health (U.S.)
Center for Biologics Evaluation and Research (U.S.)
Note At head of title: Guidance for industry and FDA staff
Gpo Item No. 0499-T-02 (online)
Sudoc No. HE 20.4802:F 73/2

 
    
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