FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Eclipse DermaFlex Cannula
K Number: K200017
·
Decision Nov 5, 2020
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
4
Review Days
307
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Basic Information
- Device Name
- Eclipse DermaFlex Cannula
- K Number
- K200017
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 880.5570
- Medical Specialty
- General Hospital
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Eclipse Medcorp, LLC
- Date Received
- January 3, 2020
- Decision Date
- November 5, 2020
- Product Code
- FMI
- 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 |
|---|---|---|---|
| FMI | Needle, Hypodermic, Single Lumen | FDA class 2 | General Hospital |
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