FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CASABLANCA
K Number: K841600
·
Decision Nov 29, 1984
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
2
Review Days
225
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Basic Information
- Device Name
- CASABLANCA
- K Number
- K841600
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5300
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- Arcon Corp.
- Date Received
- April 18, 1984
- Decision Date
- November 29, 1984
- 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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Other Clearances by Arcon Corp.
| K Number | Device Name | ||
|---|---|---|---|
| K874383 | MENTOR PLUS (CONDOM) | Mar 7, 1988 | Substantially Equivalent |