FDA PMA
FDA Class 2
Approved
🇺🇸 United States
Accessories, Soft Lens Products
PMA: P860023
·
Supplement: S010
·
Decision Sep 27, 1996
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Accessories, Soft Lens Products
- Trade Name
- BAUSCH & LOMB(R) RENU(R) MULTI-PURPOSE SOLUTION
- PMA Number
- P860023
- Supplement Number
- S010
- 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
- September 27, 1996
- Date Received
- April 3, 1996
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR MODIFYING THE CURRENT EYE CARE PRACTITIONER TRIAL LENS DISINFECTION AND STORAGE INSTRUCTIONS TO EXTEND THE MAXIMUM RECOMMENDED STORAGE TIME FROM THE CURRENTLY APPROVED 7 DAYS TO 30 DAYS IN BAUSCH & LOMB RE NU MULTI-PURPOSE SOLUTION. ALL OTHER ASPECTS OF THE LABELING REMAIN UNCHANGED FROM THOSE PREVIOUSLY APPROVED
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 |