Everlife Medical Equipment Co., Ltd.
Everlife Medical Equipment Co., Ltd. appears in FDA public data with 0 recalls, 3 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 27, 2007.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K071624 | EVERELIFE TRANSCUTANEOUS MUSCLE STIMULATOR | November 27, 2007 |
| K071320 | EVERLIFE POWERED MUSCLE STIMULATOR, MODEL E-100204, E-100504, E-100509, E-100804, E-201111, E-201211 | August 17, 2007 |
| K070890 | EVERLIFE INTERFERENTIAL CURRENT THERAPY, MODEL IF-100507 | June 29, 2007 |