World Precision 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 |
|---|
| K883869 | DERMTRODE | September 30, 1988 |
| K852289 | MODEL SA3 ESOPHAGEAL PH ELECTRODE | July 25, 1985 |