|
Device | LATITUDE PATIENT MANAGEMENT SYSTEM MODEL 6482 |
Generic Name | Implantable cardioverter defibrillator (non-CRT) |
Applicant | BOSTON SCIENTIFIC 4100 Hamline Avenue North St. Paul, MN 55112 |
PMA Number | P910077 |
Supplement Number | S062 |
Date Received | 05/25/2006 |
Decision Date | 06/23/2006 |
Product Code |
LWS |
Advisory Committee |
Cardiovascular |
Supplement Type | Special (Immediate Track) |
Supplement Reason | Labeling Change - Indications/instructions/shelf life/tradename |
Expedited Review Granted? | No |
Combination Product | No |
Recalls | CDRH Recalls |
Approval Order Statement APPROVAL TO MODIFY THE INSTRUCTIONS FOR THE LATITUDE CLINICIAN MANUAL. |