Berthold Analytical 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 |
|---|
| K872324 | LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT | August 19, 1987 |
| K870115 | BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS | March 31, 1987 |