CDRH New Update

CDRHNew

Date: March 16, 2017

The following new items were added to the CDRH web pages on March 15, 2017. Previous CDRH New Items can be found on the CDRHNew Page.

• Federal Register: Agency Information Collection Activities; Proposed Collection; Comment Request; Food and Drug Administration Safety Communication Readership Survey
• Federal Register: Agency Information Collection Activities; Proposed Collection; Comment Request; Safety Assurance Case
• Federal Register: Agency Information Collection Activities; Submission for Office of Management and Budget Review; Comment Request; Testing Communications on Medical Devices and Radiation-Emitting Products
• Federal Register: Agency Information Collection Activities; Submission for OMB Review; Comment Request; Recommended Glossary and Educational Outreach To Support Use of Symbols on Labels and in Labeling of In Vitro Diagnostic Devices Intended for Professional Use
• Federal Register: Agency Information Collection Activities; Submission for OMB Review; Comment Request; Requirement for Submission of Information on Pediatric Subpopulations That Suffer From a Disease or Condition That a Device Is Intended To Treat, Diagnose, or Cure
• Check the CDRH Customer Satisfaction Results
• Evaluation of Automatic Class III Designation (De Novo) Summaries (DEN140038 and DEN130011 added)
• Meeting materials posted for March 17, 2017 Ophthalmic Devices Panel of the Medical Devices Advisory Committee