Electro-Kinetic Eng/Mfg
Electro-Kinetic Eng/Mfg appears in FDA public data with 0 recalls, 1 510(k) clearance, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 26, 1981.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 1
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K770791 | DEPILATOR, DERMA-I & DERMA-II | January 26, 1981 |