Lifeline Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K810617 | MOBILE MATIC AUTOMATIC DONOR SCALE | April 7, 1981 |
| K760743 | DONORMATIC (BLOOD COLLECTION DEVICE) | December 6, 1976 |