FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Lens, Contact (Rigid Gas Permeable), Extended Wear
PMA: P870024
·
Supplement: S052
·
Decision Jul 3, 2019
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Lens, Contact (Rigid Gas Permeable), Extended Wear
- Trade Name
- FluoroPerm 92, FluoroPerm 60, FluoroPerm 30, FluoroPerm 151, HDS and HDS 100
- PMA Number
- P870024
- Supplement Number
- S052
- Device Class
- FDA Class 3
- Product Code
- MWL
- Generic Name
- Lens, contact (rigid gas permeable), extended wear
- Regulation Number
- 886.5916
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- July 3, 2019
- Date Received
- June 7, 2019
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Removal of a quality control batch release test.
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 |
|---|---|---|---|
| MWL | Lens, Contact (Rigid Gas Permeable), Extended Wear | FDA class 3 | Ophthalmic |