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Request for Nominations for Voting Members on Public Advisory Panels or Committees http://1.usa.gov/XdIkjh
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Webinar - Improved Access to Dev Info: What a UDI Sys can do 4 Patients & Consumers, 2/26/13 http://1.usa.gov/VJT3nI
#fda#medicaldevice -
Class II Special Controls Draft Guideline: Temporary Mandibular Condyle Reconstruction Plate http://1.usa.gov/WCCt5P
#fda#medicaldevice -
Medical Device User Fee Cover Sheet, Form FDA 3601; Comment Request http://1.usa.gov/WCBFOp
#fda#medicaldevice -
Administrative Detention & Banned Medical Devices; Comment Request http://1.usa.gov/XS5VUM
#fda#medicaldevice -
Inspection by Accredited Persons Program - OMB comment request http://1.usa.gov/YGWrk7
#fda#medicaldevice -
Accessible Med Dev Labeling in Standard Content & Format Wrkshp - Corrected date for submissions http://1.usa.gov/WDbcBd
#fda#medicaldevice -
Electronic Study Data Submission; Data Standard Support End Date http://1.usa.gov/YeKo9M
#fda#medicaldevice -
2013 Assuring Radiation Protection - Availability of Grant Funds http://1.usa.gov/UxIelX
#fda#medicaldevice -
Ophthalmic Devices - Classification of the Scleral Plug http://1.usa.gov/112yOUw
#fda#medicaldevice -
Guidance - Humanitarian Use Device (HUD) Designations http://1.usa.gov/10WaHXA
#fda#medicaldevice -
Electronic Submission Process for Requesting Export Certificates From CDRH http://1.usa.gov/W2l4Fs
#fda#medicaldevice -
Current Good Manufacturing Practice Requirements for Combination Products http://1.usa.gov/10N0Ces
#fda#medicaldevice -
Folks, our content system had a blip earlier and missing material is now coming back online. It might take an hour or so.
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Performance Eval of Accreditation Bodies under MQSA - 2011 Report to Congress http://1.usa.gov/Wj9iDr
#fda#medicaldevice#mammography -
#Cardiovascular Devices; Reclassification of External#Cardiac Compressor http://1.usa.gov/XjYztB#fda#medicaldevice -
Reclassification of Membrane Lung for Long-Term Pulmonary Support http://1.usa.gov/UAxCzH
#fda#medicaldevice -
Public Wrkshp - Accessible Med Dev Labeling in a Standard Content & Format, 4/29-30/13 http://1.usa.gov/VQvFPW
#fda#medicaldevice -
Guidance - Refuse to Accept Policy for 510(k)s http://1.usa.gov/PdyCt7
#fda#medicaldevice -
Guidance - eCopy Program for Medical Device Submissions http://1.usa.gov/Qr4h8l
#fda#medicaldevice
FDA/CDRH Industry
U.S. FDA
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