FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Gases Used Within Eye To Place Pressure On Detached Retina
PMA: P900066
·
Supplement: S006
·
Decision Dec 10, 2002
Classifications
1
FEI Numbers
2
Registration Numbers
2
Basic Information
- Device Name
- Gases Used Within Eye To Place Pressure On Detached Retina
- Trade Name
- PERFLUOROPROPANE FOR PNEUMATIC RETINOPEXY
- PMA Number
- P900066
- Supplement Number
- S006
- Device Class
- FDA Class 3
- Product Code
- LPO
- Generic Name
- Gases used within eye to place pressure on detached retina
- Regulation Number
- 886.4270
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 10, 2002
- Date Received
- August 13, 2002
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL TO ADD A MOLECULAR SIEVE SCRUBBING STEP AT THE END OF THE GAS MANUFACTURING PROCESS.
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 |
|---|---|---|---|
| LPO | Gases Used Within Eye To Place Pressure On Detached Retina | FDA class 3 | Ophthalmic |