Premarket assessment of pediatric medical devices.
| Other author/creator | Center for Devices and Radiological Health (U.S.) |
| Other author/creator | Center for Biologics Evaluation and Research (U.S.) |
| Format | Electronic and Book |
| Publication Info | [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] |
| Description | 22 p. : digital, PDF file |
| Supplemental Content | https://purl.fdlp.gov/GPO/LPS113057 |
| Subject(s) |
Click here for more information about this title
| Variant title | At head of title: Guidance for industry and FDA staff |
| General note | Title from PDF title page (viewed on May 26, 2009). |
| General note | "Document issued on: May 14, 2004". |
| General note | Includes bibliographical references (p. 21-22). |
| General note | GPO Cataloging Record Distribution Program (CRDP). |
| Technical details | Mode of access: Internet at the FDA CBER web site. Address as of 5/26/09: http://www.fda.gov/cdrh/mdufma/guidance/1220.pdf ; current access is available via PURL. |
| GPO item number | 0499-T-02 (online) |
| Govt. docs number | HE 20.4802:P 34 |
Available Items
| Library | Location | Call Number | Status | Item Actions | |
| Joyner | Electronic Resources | Access Content Online | ✔ Available |