EVERYWAY LOW BACK PAIN RELIEF SYSTEM— 510(k) K110716
Substantially EquivalentEveryway Medical Instruments Co.,Ltd
FDA 510(k) clearance K110716 for EVERYWAY LOW BACK PAIN RELIEF SYSTEM, Substantially Equivalent on 2011-10-18. Applicant: Everyway Medical Instruments Co.,Ltd. Device class: 2.
Clearance details
- Applicant
- Everyway Medical Instruments Co.,Ltd
- Product code
- Code NUH
- Device class
- Class 2
- Regulation
- 21 CFR 882.5890
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Taipei Hsien, TW
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