H&A Mui Enterprises, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 2
- Compliance Actions
- 1
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K222587 | PatCom Distal Chip Endoscope | July 28, 2023 |
| K192691 | PatCom Single-Use Introducer | February 21, 2020 |