FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Lenses, Soft Contact, Extended Wear
PMA: P980006
·
Supplement: S005
·
Decision Feb 11, 2004
Classifications
1
FEI Numbers
56
Registration Numbers
56
Basic Information
- Device Name
- Lenses, Soft Contact, Extended Wear
- Trade Name
- PUREVISION (BALAFILCON A) VISIBILITY TINTED CONTACT LENS
- PMA Number
- P980006
- Supplement Number
- S005
- Device Class
- FDA Class 3
- Product Code
- LPM
- Generic Name
- Lenses, soft contact, extended wear
- Regulation Number
- 886.5925
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- February 11, 2004
- Date Received
- January 6, 2004
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO MODIFY THE POST-APPROVAL STUDY FOR THE DEVICE.
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 |
|---|---|---|---|
| LPM | Lenses, Soft Contact, Extended Wear | FDA class 3 | Ophthalmic |