FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705

K Number: K911272 · Decision Jul 2, 1991
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
1
Applicant Total
140
Review Days
102

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Basic Information

Device Name
ENDOSCOPIC NEEDLHOLDER CAT. NUMBER 114705
K Number
K911272
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Edward Weck, Inc.
Date Received
March 22, 1991
Decision Date
July 2, 1991
Product Code
FHG
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
FHG Bell, Circumcision

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