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

EURO-MED CLEAR-VUE DISPOSABLE VAGINAL SPECULUM

K Number: K882605 · Decision Sep 15, 1988
Classifications
1
FEI Numbers
122
Registration Numbers
122
Same Product Code
70
Applicant Total
111
Review Days
83

Basic Information

Device Name
EURO-MED CLEAR-VUE DISPOSABLE VAGINAL SPECULUM
K Number
K882605
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
BUCKMAN CO., INC.
Date Received
June 24, 1988
Decision Date
September 15, 1988
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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