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

SPECULUM, VAGINAL, NONMETAL

K Number: K120743 · Decision Mar 23, 2012
Classifications
1
FEI Numbers
114
Registration Numbers
114
Same Product Code
71
Applicant Total
111
Review Days
11

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Basic Information

Device Name
SPECULUM, VAGINAL, NONMETAL
K Number
K120743
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Welch Allyn, Inc.
Date Received
March 12, 2012
Decision Date
March 23, 2012
Product Code
HIB
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
HIB Speculum, Vaginal, Nonmetal

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