FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
CANNULA AND GENERAL PURPOSE ASPIRATOR
K Number: K873552
·
Decision Nov 25, 1987
Classifications
1
FEI Numbers
19
Registration Numbers
19
Same Product Code
23
Applicant Total
3
Review Days
107
Basic Information
- Device Name
- CANNULA AND GENERAL PURPOSE ASPIRATOR
- K Number
- K873552
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5070
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- COSMEDTECH, INC.
- Date Received
- August 10, 1987
- Decision Date
- November 25, 1987
- Product Code
- HHI
- 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 |
|---|---|---|---|
| HHI | System, Abortion, Vacuum | FDA class 2 | Obstetrics/Gynecology |
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