Oldelft Corp. of America
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K980296 | OLDELFT DIGIDELCA | April 17, 1998 |
| K973219 | AMBER DU | October 8, 1997 |
| K946128 | SIMULIX-HP | May 12, 1995 |
| K950037 | N 800 HF | February 15, 1995 |
| K932848 | SIMULIX-MC CT EXTENSION | March 22, 1994 |
| K923584 | THERAPAX DXT 300 SERIES 3 | January 15, 1993 |
| K914784 | PAPILLION PROCTOSCOPE | June 5, 1992 |
| K912466 | OLDELFT SIMULIX-MC | June 28, 1991 |
| K892659 | ELECTRODELCA | November 21, 1989 |