Swemed Laboratories, 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 |
|---|
| K862364 | NEEDLE GUIDE (FOR ULTRASOUND TRANSDUCERS) | August 19, 1986 |
| K862365 | NEEDLE FOR AMNIOCENTESIS AND CYST PUNCTURE | July 7, 1986 |