FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Device, Hemostasis, Vascular
PMA: P930038
·
Supplement: S106
·
Decision Aug 7, 2025
Classifications
1
FEI Numbers
0
Registration Numbers
0
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Basic Information
- Device Name
- Device, Hemostasis, Vascular
- Trade Name
- Angio-Seal Vascular Closure Device
- PMA Number
- P930038
- Supplement Number
- S106
- Device Class
- FDA Class 3
- Product Code
- MGB
- Generic Name
- Device, hemostasis, vascular
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- August 7, 2025
- Date Received
- July 10, 2025
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
a manufacturing change to the hemostasis cap component of the Insertion Sheath subassembly
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 |
|---|---|---|---|
| MGB | Device, Hemostasis, Vascular | FDA class 3 | Unknown |