PMA P030054S035
- Device
- EPIC II HF & ATLAS II HF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S035
- Product code
- NIK
- Decision date
- 2006-09-21
- Classification
- Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (crt-d)
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Approval order statement
- CHANGE FROM A DELTA BATTERY VOLTAGE TEST TO A DIRECT IBAT CURRENT MEASUREMENT METHOD AND THE ELIMINATION OF A 14-DAY HOLD PERIOD DURING MANUFACTURING.
Current openFDA PMA Record#
- Device
- EPIC II HF & ATLAS II HF CRT-DS
- Applicant
- ABBOTT MEDICAL
- PMA number
- P030054
- Supplement
- S035
- Product code
- NIK
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Decision date
- 2006-09-21
- Decision code
- OK30
- Date received
- 2006-08-28
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- CHANGE FROM A DELTA BATTERY VOLTAGE TEST TO A DIRECT IBAT CURRENT MEASUREMENT METHOD AND THE ELIMINATION OF A 14-DAY HOLD PERIOD DURING MANUFACTURING.