FDA PMA
FDA Class 2
Approved
🇺🇸 United States
Lens, Contact (Other Material) - Daily
PMA: P860022
·
Supplement: S050
·
Decision Mar 31, 1998
Classifications
1
FEI Numbers
36
Registration Numbers
36
Basic Information
- Device Name
- Lens, Contact (Other Material) - Daily
- Trade Name
- IPAFLUOROFOCON A AND B
- PMA Number
- P860022
- Supplement Number
- S050
- Device Class
- FDA Class 2
- Product Code
- HQD
- Generic Name
- Lens, contact (other material) - daily
- Regulation Number
- 886.5916
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 31, 1998
- Date Received
- February 20, 1998
- Supplement Type
- THIRTY DAY TRACK
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for the three additional finishing laboratories listed to become additional manufacturers and distributors of the device:Premier Contact Lens, 111 28th Avenue South, Nashville, TN 37212 and Premier Contact Lens, 3614 S.Perkins, Memphis, TN 38118.
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 |
|---|---|---|---|
| HQD | Lens, Contact (Other Material) - Daily | FDA class 2 | Ophthalmic |