Dermacare Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K882494 | ELAN-E DISPOSALBE DRAPE | July 8, 1988 |
| K882421 | INFANT ELECTROSURGICAL DISPERSIVE ELECTRODE | June 30, 1988 |
| K871910 | SURGITEK DISPOSABLE BIPOLAR CORD | June 1, 1987 |
| K863279 | SURGI-TEK TUBE POSITIONER | September 9, 1986 |
| K863280 | DERMAMARKER | September 9, 1986 |
| K863278 | SURGI-WIPES | September 2, 1986 |
| K862367 | PRO-CLEAN | July 8, 1986 |
| K853374 | CORRECT-A-COUNT | September 5, 1985 |