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
HDC Tenaculum, Uterine

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