PARADYM RF VR 9250 PARADYM RF DR 9550
FDA premarket approval P980049/S102 · decided 2014-11-06
Approval details
- PMA number
- P980049
- Supplement
- S102
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- PARADYM RF VR 9250 PARADYM RF DR 9550
- Generic name
- Pacemaker/icd/crt non-implanted components
- Applicant
- MicroPort CRM USA, Inc.
- Date received
- 2014-09-15
- Decision date
- 2014-11-06
- Days to decision
- 52 days
- Decision code
- APPR
- Product code
- OSR
- Advisory committee
- Cardiovascular
- Expedited review
- No
- Location
- Arlington, TN
- Statement
- APPROVAL FOR A CHANGE TO THE SOFTWARE CODE FOR THE SMARTVIEW(HOME) MONITOR USED FOR THE DEVICES.
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