PMA P890048S005
- Device
- USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
- Applicant
- Usci, Div. C.R. Bard, Inc.
- PMA number
- P890048
- Supplement
- S005
- Product code
- LOX
- Decision date
- 1996-11-26
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Approval order statement
- MODIFICATION TO THE PACKAGE TRAY OF THE USCI(R) PROBE(TM) III BALLOON-ON-A-WIRE(TM) DILATATION SYSTEM
Current openFDA PMA Record#
- Device
- USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
- Applicant
- Usci, Div. C.R. Bard, Inc.
- PMA number
- P890048
- Supplement
- S005
- Product code
- LOX
- Generic name
- Catheters, transluminal coronary angioplasty, percutaneous
- Decision date
- 1996-11-26
- Decision code
- APPR
- Date received
- 1996-09-05
- Supplement type
- Normal 180 Day Track
- Supplement reason
- Change Design/Components/Specifications/Material
- Approval order statement
- MODIFICATION TO THE PACKAGE TRAY OF THE USCI(R) PROBE(TM) III BALLOON-ON-A-WIRE(TM) DILATATION SYSTEM