FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Pacemaker/Icd/Crt Non-Implanted Components
PMA: P890003
·
Supplement: S344
·
Decision Feb 5, 2016
Classifications
1
FEI Numbers
34
Registration Numbers
34
Basic Information
- Device Name
- Pacemaker/Icd/Crt Non-Implanted Components
- Trade Name
- MEDTRONIC CARELINK MONITOR, MYCARELINK PATIENT MONITOR
- PMA Number
- P890003
- Supplement Number
- S344
- Device Class
- FDA Class 3
- Product Code
- OSR
- Generic Name
- Pacemaker/icd/crt non-implanted components
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- February 5, 2016
- Date Received
- November 16, 2015
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for the Alert Management Feature for the CareLink Network.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OSR | Pacemaker/Icd/Crt Non-Implanted Components | FDA class 3 | Unknown |