Health Development Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K830397 | PEM-C | April 12, 1983 |
| K823937 | SEMINAL COLLECTION DEVICE | February 24, 1983 |
| K810499 | PERCUTANEOUS GASTROINTESTINAL TUBE | March 4, 1981 |
| K802482 | KEOFEED (R) EASY-FILL ENTERIC FEED BAG | October 31, 1980 |
| K791714 | SURGIFEED | January 16, 1980 |