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- MiscellaneousMiscellaneous
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- K200636AXUS ES-5 Electro-Acupuncture DeviceUCleared 510(K)
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Show All 22 Submissions
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- NPEMaterial, Embolization, Neurovascular, Polymerizing Or Precipitating3Product Code
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- Submissions with No Product CodeMiscellaneous
- Subpart B—Cardiovascular Diagnostic DevicesCFR Sub-Part
- Subpart B—Diagnostic DevicesCFR Sub-Part
- Subpart B—Neurological Diagnostic DevicesCFR Sub-Part
- Subpart B—Physical Medicine Diagnostic DevicesCFR Sub-Part
- Subpart C—Cardiovascular Monitoring DevicesCFR Sub-Part
- Subpart D—Physical Medicine Prosthetic DevicesCFR Sub-Part
- Subpart E—Neurological Surgical DevicesCFR Sub-Part
- Subpart E—Surgical DevicesCFR Sub-Part
- Subpart F—Cardiovascular Therapeutic DevicesCFR Sub-Part
- Subpart F—Neurological Therapeutic DevicesCFR Sub-Part
- Subpart F—Physical Medicine Therapeutic DevicesCFR Sub-Part
- Subpart F—Therapeutic DevicesCFR Sub-Part
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AXUS ES-5 Electro-Acupuncture Device
- Page Type
- Cleared 510(K)
- FDA Hosted PDF* The FDA doesn't provide PDFs for all submissions.
- 510(k) Number
- K200636
- 510(k) Type
- Traditional
- Applicant
- Lhasa OMS, INC.
- Country
- United States
- FDA Decision
- Substantially Equivalent
- Decision Date
- 2/3/2021
- Days to Decision
- 330 days
- Submission Type
- Summary