FDA PMA
FDA Class 2
Approved
🇺🇸 United States
Accessories, Soft Lens Products
PMA: P960012
·
Supplement: S001
·
Decision Apr 24, 1997
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Accessories, Soft Lens Products
- Trade Name
- REFRESH CL(TM)/LUBRICATING AND REWETING DROPS
- PMA Number
- P960012
- Supplement Number
- S001
- Device Class
- FDA Class 2
- Product Code
- LPN
- Generic Name
- Accessories, soft lens products
- Regulation Number
- 886.5928
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- April 24, 1997
- Date Received
- December 23, 1996
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO ADD RIGID GAS PERMEABLE CONTACT LENSES TO THE LABEL INDICATIONS.
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 |
|---|---|---|---|
| LPN | Accessories, Soft Lens Products | FDA class 2 | Ophthalmic |