FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CERVILENZ UTERINE MEASURING SOUND

K Number: K011840 · Decision Aug 10, 2001
Classifications
1
FEI Numbers
132
Registration Numbers
132
Same Product Code
9
Applicant Total
1
Review Days
59

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Basic Information

Device Name
CERVILENZ UTERINE MEASURING SOUND
K Number
K011840
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.4530
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cervilenz, Inc.
Date Received
June 12, 2001
Decision Date
August 10, 2001
Product Code
HHM
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
HHM Sound, Uterine

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