FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: P040045
·
Supplement: S025
·
Decision Oct 12, 2011
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- VISTAKON (SENOFILCON A) BRAND CONTACT LENSES
- PMA Number
- P040045
- Supplement Number
- S025
- Device Class
- FDA Class 3
- Product Code
- LPM
- Generic Name
- Lenses, soft contact, extended wear
- Regulation Number
- 886.5925
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 12, 2011
- Date Received
- September 12, 2011
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
UPGRADE TO THE SALINE DOSE HEAD DURING THE MANUFACTURING OF THE DEVICE.
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 |
|---|---|---|---|
| LPM | Lenses, Soft Contact, Extended Wear | FDA class 3 | Ophthalmic |