FDA 510(k)
FDA class 2
Unknown
🇺🇸 United States
RedDrop ONE (One)
K Number: K234081
·
Decision Mar 21, 2024
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
1
Review Days
90
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Basic Information
- Device Name
- RedDrop ONE (One)
- K Number
- K234081
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4850
- Medical Specialty
- General, Plastic Surgery
- Decision
- Unknown
- Statement or Summary
- Summary
- Applicant
- Reddrop DX
- Date Received
- December 22, 2023
- Decision Date
- March 21, 2024
- Product Code
- FMK
- Advisory Committee
- General, Plastic Surgery
- 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 |
|---|---|---|---|
| FMK | Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature | FDA class 2 | General, Plastic Surgery |
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