Baka Manufacturing Co., 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 |
|---|
| K781800 | GRIP, HOSPITAL UTILITY | December 7, 1978 |
| K780190 | CATHETER STRAP & RUINARY BAY HOLDER | February 21, 1978 |