William Harvey Life Products Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K811703 | CARDIFF ALDASORBER SYSTEM | June 16, 1981 |
| K810065 | SCOTT CM42 PASTEURIZER | January 28, 1981 |
| K770720 | TUBING PACK, EXTRACORPOREAL, H-3000 | August 4, 1977 |