FDA 510(k)
FDA class 2
Substantially Equivalent
🇵🇰 Pakistan
UTERINE TENACLUM HOOK
K Number: K001818
·
Decision Aug 30, 2000
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
19
Applicant Total
1
Review Days
76
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Basic Information
- Device Name
- UTERINE TENACLUM HOOK
- K Number
- K001818
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 884.4530
- Medical Specialty
- Obstetrics/Gynecology
- Decision
- Substantially Equivalent
- Statement or Summary
- Statement
- Applicant
- Towne Brothers (Pvt.), Ltd.
- Date Received
- June 15, 2000
- Decision Date
- August 30, 2000
- Product Code
- HDC
- 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 |
|---|---|---|---|
| HDC | Tenaculum, Uterine | FDA class 2 | Obstetrics/Gynecology |
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