FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Genteel Lancing Device
K Number: K153670
·
Decision May 12, 2016
Classifications
1
FEI Numbers
157
Registration Numbers
157
Same Product Code
109
Applicant Total
1
Review Days
143
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Basic Information
- Device Name
- Genteel Lancing Device
- K Number
- K153670
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4850
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Genteel, LLC
- Date Received
- December 21, 2015
- Decision Date
- May 12, 2016
- 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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