FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
NEUTROPHASE
K Number: K081009
·
Decision May 20, 2008
Classifications
1
FEI Numbers
79
Registration Numbers
79
Same Product Code
221
Applicant Total
3
Review Days
42
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Basic Information
- Device Name
- NEUTROPHASE
- K Number
- K081009
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 880.5090
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Novabay Pharmaceuticals
- Date Received
- April 8, 2008
- Decision Date
- May 20, 2008
- Product Code
- KMF
- Advisory Committee
- General Hospital
- Review Advisory Committee
- SU
- 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 |
|---|---|---|---|
| KMF | Bandage, Liquid | FDA class 1 | General Hospital |
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