FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
StimSite
K Number: K200886
·
Decision Nov 10, 2020
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
96
Applicant Total
1
Review Days
222
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Basic Information
- Device Name
- StimSite
- K Number
- K200886
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 874.1820
- Medical Specialty
- Ear, Nose, Throat
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Allotrope Medical, Inc.
- Date Received
- April 2, 2020
- Decision Date
- November 10, 2020
- Product Code
- ETN
- Advisory Committee
- Ear, Nose, Throat
- Review Advisory Committee
- OB
- 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 |
|---|---|---|---|
| ETN | Stimulator, Nerve | FDA class 2 | Ear, Nose, Throat |
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