FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Aid, Surgical, Viscoelastic
PMA: P810031
·
Supplement: S040
·
Decision Aug 31, 2011
Classifications
1
FEI Numbers
27
Registration Numbers
27
Basic Information
- Device Name
- Aid, Surgical, Viscoelastic
- Trade Name
- SODIUM HYALURONATE OPHTHALMIC VISCOELASTIC DEVICES
- PMA Number
- P810031
- Supplement Number
- S040
- Device Class
- FDA Class 3
- Product Code
- LZP
- Generic Name
- AID, SURGICAL, VISCOELASTIC
- Regulation Number
- 886.4275
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- August 31, 2011
- Date Received
- August 1, 2011
- Supplement Type
- 30-Day Notice
- Expedited Review
- N
Advisory Committee Statement
IMPLEMENTATION OF A NEW PURE STEAM GENERATOR.
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 |
|---|---|---|---|
| LZP | Aid, Surgical, Viscoelastic | FDA class 3 | Ophthalmic |