FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
PLEASURE PLUS
K Number: K902772
·
Decision Aug 14, 1991
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
4
Review Days
418
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Basic Information
- Device Name
- PLEASURE PLUS
- K Number
- K902772
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5300
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- Medimix Products, Inc.
- Date Received
- June 22, 1990
- Decision Date
- August 14, 1991
- Product Code
- HIS
- 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 |
|---|---|---|---|
| HIS | Condom | FDA class 2 | Obstetrics/Gynecology |
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