FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
Trojan Chain Reaction Personal Lubricant
K Number: K161544
·
Decision Aug 31, 2016
Classifications
1
FEI Numbers
123
Registration Numbers
123
Same Product Code
242
Applicant Total
29
Review Days
89
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Basic Information
- Device Name
- Trojan Chain Reaction Personal Lubricant
- K Number
- K161544
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5300
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Church & Dwight Co., Inc.
- Date Received
- June 3, 2016
- Decision Date
- August 31, 2016
- 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 |
Similar 510(k) Clearances
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