FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SpringTMS
K Number: K182976
·
Decision Feb 25, 2019
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
5
Applicant Total
1
Review Days
122
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Basic Information
- Device Name
- SpringTMS
- K Number
- K182976
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 882.5808
- Medical Specialty
- Neurology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Eneura®, Inc.
- Date Received
- October 26, 2018
- Decision Date
- February 25, 2019
- Product Code
- OKP
- Advisory Committee
- Neurology
- Review Advisory Committee
- NE
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| OKP | Transcranial Magnetic Stimulator For The Treatment Of Migraine Headache | FDA class 2 | Neurology |
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