FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Ventricular (Assist) Bypass
PMA: P100047
·
Supplement: S167
·
Decision Jul 15, 2020
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Ventricular (Assist) Bypass
- Trade Name
- HeartWare Ventricular Assist System
- PMA Number
- P100047
- Supplement Number
- S167
- Device Class
- FDA Class 3
- Product Code
- DSQ
- Generic Name
- Ventricular (assist) bypass
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- July 15, 2020
- Date Received
- June 19, 2020
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Replace the existing recording system for monitoring parameters in the manufacturing areas and water system with an automated environmental monitoring application at the Miami Lakes facility.
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 |
|---|---|---|---|
| DSQ | Ventricular (Assist) Bypass | FDA class 3 | Unknown |