Premarket Approval (PMA)

Note: this medical device has supplements. The device description/function or indication may have changed. Be sure to look at the supplements to get an up-to-date information on device changes. The labeling included below is the version at time of approval of the original PMA or panel track supplement and may not represent the most recent labeling.

• Device: MODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER
• Generic Name: Generator, pulse, pacemaker, external programmable (for electrophysiological studies only)
• Regulation Number: 870.1750
• Applicant: PACE MEDICAL; 391 TOTTEN POND RD.; WALTHAM, MA 02451
• PMA Number: P920032
• Date Received: 06/30/1992
• Decision Date: 03/10/1994
• Product Code: JOQ
• Docket Number: 94M-0129
• Notice Date: 05/06/1994
• Advisory Committee: Cardiovascular
• Expedited Review Granted?: No
• Combination Product: No
• Supplements: S001 S002 S003 S004 S005 S006 S007 S008