ELECTROMED REUSABLE NEUROSTIMULATION ELECTRODES— 510(k) K030800
Substantially EquivalentEletromed, Inc.
FDA 510(k) clearance K030800 for ELECTROMED REUSABLE NEUROSTIMULATION ELECTRODES, Substantially Equivalent on 2003-06-11. Applicant: Eletromed, Inc.. Device class: 2.
Clearance details
- Applicant
- Eletromed, Inc.
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Betheda, MD, US
Recent devices under product code GXY
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Data sourced from openFDA. This site is unofficial and independent of the FDA.