Bioject, Inc.
Bioject, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Apr 2, 2009.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K090003 | ZETAJET | Apr 2, 2009 |
| K050734 | COOL.CLICK | Jun 3, 2005 |
| K010623 | RECONSTITUTION KIT & VIAL CONNECTOR | Apr 5, 2001 |
| K003908 | SEROJET | Mar 8, 2001 |
| K994384 | CLICKER | Jun 22, 2000 |
| K960373 | BIOJECTOR 2000 MODEL 1B02000 | Mar 5, 1997 |
| K963012 | BIOJECT NEEDLE-FREE VIAL ADAPTER (13MM) | Oct 15, 1996 |
| K920631 | BIOJECT JET INJECTION SYSTEM | Jun 28, 1994 |
| K861687 | BIOJECTOR SYRINGE SYSTEM | Apr 23, 1987 |