FDA documents

 
Containers:
Box 22 (MS 8696)
Component identifier:
File 15
Content Summary:
[FDA application forms, Report, Correspondence, Copies of scientific papers. FDA information: IDE (Investigational Device Exemption) application form, `FDA's Premarket Guidelines', `Product Development Guidelines' November 1980; Report: `Porous transvenous ventricular tined leads study protocol - Non-invasive monitoring of threshold voltage and pacing impedance using the impedance and threshold monitoring pacemaker (IMP); Copies of scientific papers: `Comparison between in vitro and in vivo tests for carcinogenicity' by D.B. Clayton, `Methods for detecting carcinogens and mutagens with the salmonella/mammalian-microsome mutagenicity test' by B.N. Ames et al; `Application of microbiol and mammalian cells to the assessment of mutagenicity' by V.A. Ray; Inwards correspondence from: M. Hirshorn (Nucleus)] 1980-1982

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Parkes Place
Canberra ACT 2600, Australia
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