Boekel Industries, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K831592 | ANHYDRIC INCUBATORS, CULTURE INCUBATOR | June 16, 1983 |
| K823766 | BLOOD GAS INCUBATOR #260650 | February 18, 1983 |
| K822564 | WATER BATH | September 14, 1982 |