Medi-Tech Coronary Balloon Dilatation Catheter Sys
FDA premarket approval P840040 · Catheters, transluminal coronary angioplasty, percutaneous
PMA numberP840040
Approval
- Applicant
- Boston Scientific Corp
- Received
- September 5, 1984
- Decision date
- December 19, 1985 (APWD)
- Supplements
- 49, latest November 21, 1997
- Product code
- LOX – Catheters, Transluminal Coronary Angioplasty, Percutaneous