FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Intraocular Lens
PMA: P960036
·
Supplement: S003
·
Decision Sep 25, 2000
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- MEMORY LENS(R) UV ABSORBING HYDROPHILIC POSTERIOR CHAMBER IOL
- PMA Number
- P960036
- Supplement Number
- S003
- 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
- September 25, 2000
- Date Received
- August 31, 2000
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Other
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO MODIFY THE EUROPEAN PHASE-IN STUDY DESCRIBED IN SUPPLEMENT 2 DATED 8/25/00 FOR THE MEMORY LENS(R)
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 |