Cormed, Inc., Sub. C.R.Bard, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K863606 | BUTTERFLY NON-CORING NEEDLE SET | December 18, 1986 |
| K860432 | PERCUTANEOUS INTRODUCER KIT | March 31, 1986 |
| K854019 | PORT-GARD | November 26, 1985 |
| K850967 | STERILE CORMED MEDIPORT | May 17, 1985 |
| K850674 | CORMED II AMBULATORY INFUSION PUMP | April 9, 1985 |
| K843083 | CORMED HUBER POINT NEEDLE | September 5, 1984 |
| K833915 | VASCULAR ACCESS CATH. REPAIR KIT | March 30, 1984 |
| K823553 | CORCATH H & B VASCULAR ACCESS CATHETER | January 5, 1983 |