PE-210AK SWITCH BOX— 510(k) K110376
Substantially EquivalentNihon Kohden Corp.
FDA 510(k) clearance K110376 for PE-210AK SWITCH BOX, Substantially Equivalent on 2011-07-29. Applicant: Nihon Kohden Corp.. Device class: 2.
Clearance details
- Applicant
- Nihon Kohden Corp.
- Product code
- Code GWQ
- Device class
- Class 2
- Regulation
- 21 CFR 882.1400
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Foothill, CA, US
Recent devices under product code GWQ
view allMore clearances from Nihon Kohden Corp.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.