FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CUROS PORT PROTECTOR
K Number: K111992
·
Decision Jan 12, 2012
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
21
Applicant Total
3
Review Days
183
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Basic Information
- Device Name
- CUROS PORT PROTECTOR
- K Number
- K111992
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5440
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Ivera Medical, Inc.
- Date Received
- July 13, 2011
- Decision Date
- January 12, 2012
- Product Code
- QBP
- 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 |
|---|---|---|---|
| QBP | Cap, Device Disinfectant | FDA class 2 | General Hospital |
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