PMA P030005S100
- Device
- INVIVE, INTUA
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S100
- Product code
- NKE
- Decision date
- 2013-07-03
- Classification
- Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (crt-p)
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Approval order statement
- AUTOMATION OF A MANUAL SIEVE PROCESS AT A SUPPLIER AND ADDITION OF A NEW REQUIREMENT TO SOURCE DOCUMENTATION FOR INCOMING ACCEPTANCE.
Current openFDA PMA Record#
- Device
- INVIVE, INTUA
- Applicant
- Guidant Corp.
- PMA number
- P030005
- Supplement
- S100
- Product code
- NKE
- Generic name
- Pulse generator, pacemaker, implantable, with cardiac resynchronization (CRT-P)
- Decision date
- 2013-07-03
- Decision code
- OK30
- Date received
- 2013-06-03
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- AUTOMATION OF A MANUAL SIEVE PROCESS AT A SUPPLIER AND ADDITION OF A NEW REQUIREMENT TO SOURCE DOCUMENTATION FOR INCOMING ACCEPTANCE.