FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Barrier, Absorbable, Adhesion
PMA: P990015
·
Supplement: S001
·
Decision Jul 9, 2002
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Barrier, Absorbable, Adhesion
- Trade Name
- GYNECARE INTERGEL ADHESION PREVENTION SOLUTION
- PMA Number
- P990015
- Supplement Number
- S001
- Device Class
- FDA Class 3
- Product Code
- MCN
- Generic Name
- Barrier, absorbable, adhesion
- Medical Specialty
- Unknown
- Advisory Committee
- Obstetrics/Gynecology
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- July 9, 2002
- Date Received
- April 18, 2002
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR AN ADDITIONAL MANUFACTURING FACILITY FOR THE BLOW/FILL/SEAL AND ASEPTIC FILLING OF THE GYNECARE INTERGEL ADHESION PREVENTION SOLUTION. THE FACILITY IS LOCATED AT CARDINAL HEALTH MANUFACTURING SERVICES, AUTOMATIC LIQUID PACKAGING, INC., WOODSTOCK, ILLINOIS.
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 |
|---|---|---|---|
| MCN | Barrier, Absorbable, Adhesion | FDA class 3 | Unknown |