FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
SWIVEL ADAPTER
K Number: K900642
·
Decision Mar 19, 1990
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
23
Applicant Total
2
Review Days
38
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Basic Information
- Device Name
- SWIVEL ADAPTER
- K Number
- K900642
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.5070
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Applicant
- Williams Specialty Products, Inc.
- Date Received
- February 9, 1990
- Decision Date
- March 19, 1990
- 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 |
Similar 510(k) Clearances
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CANNULA, SUCTION UTERINE
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Other Clearances by Williams Specialty Products, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K900641 | CANNULA, SUCTION UTERINE | Mar 30, 1990 | Substantially Equivalent |