FDA 510(k)
FDA class 2
Substantially Equivalent
🇩🇪 Germany
VENOTRAIN CURAFLOW
K Number: K111662
·
Decision Oct 4, 2011
Classifications
1
FEI Numbers
91
Registration Numbers
91
Same Product Code
63
Applicant Total
2
Review Days
112
Basic Information
- Device Name
- VENOTRAIN CURAFLOW
- K Number
- K111662
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5780
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- BAUERFEIND AG
- Date Received
- June 14, 2011
- Decision Date
- October 4, 2011
- Product Code
- DWL
- Advisory Committee
- General Hospital
- Review Advisory Committee
- HO
- 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 |
|---|---|---|---|
| DWL | Stocking, Medical Support (To Prevent Pooling Of Blood In Legs) | FDA class 2 | General Hospital |
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Other Clearances by BAUERFEIND AG
| K Number | Device Name | ||
|---|---|---|---|
| K123921 | BODYTRONIC 200 | Apr 26, 2013 | Substantially Equivalent |