PMA P880038S034

Device: MODEL 9602 PROGRAMMER
Applicant: St. Jude Medical, Inc.
PMA number: P880038
Supplement: S034
Product code: DXY
Decision date: 1997-04-29
Generic name: implantable pacemaker Pulse-generator
Approval order statement: APPROVAL FOR AN ALTERNATE MANUFACTURING SITE FOR THE MODEL 9602 PROGRAMMER. THE SITE IS LOCATED AT PACESETTER, INC., 15900 VALLEY VIEW CT., SYLMAR CA.

Current openFDA PMA Record

Device: MODEL 9602 PROGRAMMER
Applicant: St. Jude Medical, Inc.
PMA number: P880038
Supplement: S034
Product code: DXY
Generic name: implantable pacemaker Pulse-generator
Decision date: 1997-04-29
Decision code: APPR
Date received: 1997-04-24
Supplement type: Normal 180 Day Track
Supplement reason: Location Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement: APPROVAL FOR AN ALTERNATE MANUFACTURING SITE FOR THE MODEL 9602 PROGRAMMER. THE SITE IS LOCATED AT PACESETTER, INC., 15900 VALLEY VIEW CT., SYLMAR CA.