PMA P030054S216
- Device
- UNIFY FAMILY OF CRT-DS AND LEADS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S216
- Product code
- NIK
- Decision date
- 2012-03-14
- Classification
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (crt-d)
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Approval order statement
- ACCEPTANCE OF OPTIMIZED BOND PARAMETERS USED IN THE HYBRID WIRE BONDING PROCESS.
Current openFDA PMA Record#
- Device
- UNIFY FAMILY OF CRT-DS AND LEADS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S216
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2012-03-14
- Decision code
- OK30
- Date received
- 2012-02-13
- Supplement type
- 30-Day Notice
- Approval order statement
- ACCEPTANCE OF OPTIMIZED BOND PARAMETERS USED IN THE HYBRID WIRE BONDING PROCESS.