FDA PMA
FDA Class 3
Approved (Withdrawn)
🇺🇸 United States
Intraocular Lens
PMA: P820072
·
Decision Jul 21, 1983
Classifications
1
FEI Numbers
59
Registration Numbers
59
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- CIRCULAR OPEN LOOP POSTERIOR IOLS & KRATZ ELLIPTIC
- PMA Number
- P820072
- Device Class
- FDA Class 3
- Product Code
- HQL
- Generic Name
- intraocular lens
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved (Withdrawn)
- Decision Code
- APWD
- Decision Date
- July 21, 1983
- Date Received
- September 30, 1982
- Expedited Review
- N
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 |