FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Ventricular (Assist) Bypass
PMA: P160054
·
Supplement: S123
·
Decision Mar 25, 2026
Classifications
1
FEI Numbers
0
Registration Numbers
0
Research PMA P160054 in seconds
The Research Assistant summarizes PMA approval history, supplements and related safety signals — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- Ventricular (Assist) Bypass
- Trade Name
- HeartMate 3 Left Ventricular Assist System
- PMA Number
- P160054
- Supplement Number
- S123
- 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
- March 25, 2026
- Date Received
- February 27, 2026
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
the addition of new laser welding equipment used in the manufacturing of the HeartMate 3 LVAD hermetic motor enclosure assembly
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 |