• 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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
Note: this medical device has supplements. The device description may have changed. Be sure to look at the supplements to get an up-to-date view of this device.
 
Trade NameSENSOLOG MODEL 703 PULSE GENERATOR & P700 PROGRAMM
Classification Nameimplantable pacemaker pulse-generator
Generic Namepulse generator and programmer
Regulation Number870.3610
ApplicantST. JUDE MEDICAL, INC.
PMA NumberP880006
Date Received02/05/1988
Decision Date02/28/1989
Product Code
DXY[ Registered Establishments with DXY ]
Docket Number 89M-0089
Notice Date 04/18/1989
Advisory Committee Cardiovascular
Expedited Review Granted? No
Combination Product No
Supplements: S001 S002 S004 S005 S006 S007 
S008 S009 S010 S011 S012 S013 
S014 S016 S017 S018 S020 S021 
S022 S023 S024 S025 S026 S027 
S028 S029 S030 S031 S032 S033 
S034 S036 S037 S038 S039 S040 
S041 S043 S044 S045 S046 S047 
S048 S049 S050 S051 S052 S053 
S054 S055 S056 S057 S058 S059 
S060 S061 S062 S063 S064 S065 
S066 S067 S068 S069 S070 S071 
S072 S073 S074 S075 S076 S078 
S079 S080 S082 S083 S086 
-
-