FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intraocular Lens
PMA: P790027
·
Supplement: S067
·
Decision May 21, 2002
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- PMMA INTRAOCULAR LENS
- PMA Number
- P790027
- Supplement Number
- S067
- Device Class
- FDA Class 3
- Product Code
- HQL
- Generic Name
- intraocular lens
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- May 21, 2002
- Date Received
- April 8, 2002
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Express GMP Supplement
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A NEW MANUFACTURING FACILITY LOCATED AT BAUSCH & LOMB, INC. WILMINGTON, MASSACHUSETTS. THE CLEAR COMPRESSION MOLDED BLANK PMMA MATERIAL WILL BE MANUFACTURED AT THIS FACILITY.
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 |
|---|---|---|---|
| HQL | Intraocular Lens | FDA class 3 | Ophthalmic |