FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
POISE PERSONAL LUBRICANT
K Number: K120650
·
Decision Jul 11, 2012
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
242
Applicant Total
11
Review Days
131
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Basic Information
- Device Name
- POISE PERSONAL LUBRICANT
- K Number
- K120650
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5300
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Kimberly-Clark Corporation
- Date Received
- March 2, 2012
- Decision Date
- July 11, 2012
- Product Code
- NUC
- Advisory Committee
- Obstetrics/Gynecology
- Review Advisory Committee
- OB
- 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 |
|---|---|---|---|
| NUC | Lubricant, Personal | FDA class 2 | Obstetrics/Gynecology |
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