FDA documents
- Containers:
- Box 19 (MS 8696)
- Component identifier:
- File 1
- Content Summary:
- [Reports, Patient consent forms, Correspondence. Reports include: `Clinical trial protocol for patients receiving a multiple-channnel cochlear implant', `Device exemption to the Food and Drug Administration for a significant risk device', `FDA guidelines on preparing reports'; Patient consent forms: `Informed patient consent regarding a clinical investigation study of implantable hearing prosthesis required by USA Food and Drug Administration'; Inwards and outwards correspondence with: P.K. Wood (University of Melbourne), C. Bunn, R.K. Shepherd (UNDOL)] 1982
Access and use
- Location of this collection:
-
Parkes PlaceCanberra ACT 2600, Australia
- Contact: