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

HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140

K Number: K900618 · Decision Apr 25, 1990
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
59
Applicant Total
23
Review Days
76

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Basic Information

Device Name
HUNTLEIGH FETAL DOPPLER, FD-1 & DOPCORD, D140
K Number
K900618
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2660
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Huntleigh Technology, Inc.
Date Received
February 8, 1990
Decision Date
April 25, 1990
Product Code
KNG
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
KNG Monitor, Ultrasonic, Fetal

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