Staodynamics, Inc.
Staodynamics, Inc. appears in FDA public data with 0 recalls, 14 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 24, 1985.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 14
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K852298 | TENS-AID STERILE ELECTRODES FOR POST-OP TENS | Jun 24, 1985 |
| K843964 | TENS-AID PREMIUM ELECTRODES | Feb 25, 1985 |
| K832988 | STAODYN EMS/PLUS | Nov 22, 1983 |
| K813283 | 10D (TENS DEVICE) | Feb 10, 1982 |
| K813098 | TENS DEVICE | Nov 20, 1981 |
| K811345 | INSIGHT | Jul 10, 1981 |
| K792529 | POINT LOCATOR STIMULATOR | Feb 26, 1980 |
| K792501 | PLS MINI | Feb 26, 1980 |
| K800068 | ELECTRICAL MUSCLE STIMULATOR (EMS) | Feb 5, 1980 |
| K792502 | TENS 4100 | Dec 18, 1979 |
| K792474 | TENS 4500 | Dec 13, 1979 |
| K791087 | PORTABLE PULSE GALVANIC STIMULATOR | Oct 12, 1979 |
| K790542 | ELECTRODES, STAODERM STERILE | May 23, 1979 |
| K790904 | STAO-HOTPACK | May 18, 1979 |