Newport Biosystems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K881648 | TRANSFER CONTAINER HUMIDIFIER | December 30, 1988 |
| K860282 | RPMI 1640 W/GLUTAMINE W/HEPES | February 5, 1986 |
| K855085 | TISSUE CULTURE MEDIA | January 13, 1986 |
| K853441 | FETAL BOVINE SERUM IN TRANSFER CONTAINER | August 26, 1985 |