INWAVE— 510(k) K121820
Substantially EquivalentZynex Medical, Inc.
FDA 510(k) clearance K121820 for INWAVE, Substantially Equivalent on 2012-08-24. Applicant: Zynex Medical, Inc.. Device class: 2.
Clearance details
- Applicant
- Zynex Medical, Inc.
- Product code
- Code KPI
- Device class
- Class 2
- Regulation
- 21 CFR 876.5320
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Location
- Lone Tree, CO, US
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More clearances from Zynex Medical, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.