FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Ventricular (Assist) Bypass
PMA: P100047
·
Supplement: S062
·
Decision Jul 2, 2015
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
- S062
- 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 2, 2015
- Date Received
- June 3, 2015
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
IMPLEMENTATION OF AN ADHESIVE DISPENSER DURING THE ASSEMBLY OF THE HEARTWARE VENTRICULAR ASSIST DEVICE HOUSING.
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 |