DUAL CHAMBER IMPLANTABLE CARDIOVERTER
FDA premarket approval P030054/S009 · decided 2005-05-09
Approval details
- PMA number
- P030054
- Supplement
- S009
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- DUAL CHAMBER IMPLANTABLE CARDIOVERTER
- Generic name
- Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
- Applicant
- ABBOTT MEDICAL
- Date received
- 2005-04-21
- Decision date
- 2005-05-09
- Days to decision
- 18 days
- Decision code
- OK30
- Product code
- NIK
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Sylmar, CA
- Statement
- ALTERNATE PROCESS FOR REMOVING EPOXY FROM THE CONNECTOR BLOCK THREADED BORES OF THE ICD DEVICES.
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