FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SiteSeal Femoral Compression Device
K Number: K192413
·
Decision Mar 31, 2020
Classifications
1
FEI Numbers
186
Registration Numbers
186
Same Product Code
203
Applicant Total
1
Review Days
209
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Basic Information
- Device Name
- SiteSeal Femoral Compression Device
- K Number
- K192413
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 870.4450
- Medical Specialty
- Cardiovascular
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ensite Vacular, LLC
- Date Received
- September 4, 2019
- Decision Date
- March 31, 2020
- Product Code
- DXC
- Advisory Committee
- Cardiovascular
- Review Advisory Committee
- CV
- 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 |
|---|---|---|---|
| DXC | Clamp, Vascular | FDA class 2 | Cardiovascular |
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