• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Premarket Approval (PMA)

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | Registration & Listing | Adverse Events | Recalls | PMA | Classification | Standards | Inspections
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameDIAPHRAGMATIC PACEMAKER PHRENIC NERVE
Classification Nameimplanted diaphragmatic/phrenic nerve stimulator
Generic Namestimulator, diaphragmatic/phrenic nerve, implant
Regulation Number882.5830
ApplicantAVERY LABORATORIES, INC.
PMA NumberP860026
Supplement NumberS006
Date Received04/27/2000
Decision Date07/07/2000
Product Code
GZE
Advisory Committee Cardiovascular
Supplement Typenormal 180 day track
Supplement Reason process change: sterilization
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for process validation of the proposed device sterilization procedure, proposed labeling for the device packaging, and the proposed changes to the instruction manual. The device, as modified, will be marketed under the trade name mark iv and is indicated for persons who require chronic ventilatory support because oof upper motor neuron respiratory muscle paralysis (rmp) or because of central alveolar hypoventilation (cah) and whose remaining phrenic nerve, lung, and diaphragm function.
-
-