Hi-Dow International, Inc.
Hi-Dow International, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 19, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K233461 | Hi-Dow PRO TOUCH WIRELESS 6-12 (HD-19A) | January 19, 2024 |
| K210383 | Wrap Accessory Electrodes | November 12, 2021 |
| K202337 | Pulsed electromagnetic field wrap | December 15, 2020 |
| K190617 | Wrap accessory electrodes | July 2, 2019 |
| K163393 | Hi-Dow Wireless TENS/EMS System (Model HD-5N) | August 4, 2017 |
| K102598 | HI-DOW-XP | May 13, 2011 |