Stiefel Research Institute, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K914591 | L.C.S. 2000 SYSTEM | January 14, 1992 |
| K910216 | STEADFAST DENTURE ADHESIVE POWDER | March 29, 1991 |
| K895818 | STEADFAST DENTURE ADHESIVE CREAM | April 3, 1990 |
| K895817 | HERMAL WOUND CARE KIT | January 19, 1990 |
| K896724 | CRYOJET LIQUID NITROGEN SPRAY CRYOSURGICAL INSTRU. | January 9, 1990 |
| K893996 | CUSIS ULTRASOUND SKIN IMAGING SYSTEM | September 21, 1989 |