Knight Medical, Inc.
Knight Medical, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 4, 1993.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K921127 | PANDA NEEDLE CATHETER JEJUNOSTOMY KIT | January 4, 1993 |
| K903086 | TUBE GASTROSTOMY | November 20, 1990 |
| K883848 | KMI OXY-BAN | March 2, 1989 |
| K883886 | DOUBLE CLOSED URINARY DRAINAGE SYSTEM | December 19, 1988 |
| K862489 | ENTERAL FEEDING SETS FOR GRAVITY AND PUMP USE | September 23, 1986 |