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

MULTI DOPPLEX II / FETAL DOPPLEX II

K Number: K930200 · Decision Jun 24, 1994
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
59
Applicant Total
14
Review Days
526

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Basic Information

Device Name
MULTI DOPPLEX II / FETAL DOPPLEX II
K Number
K930200
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2660
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Huntleigh Healthcare, Inc.
Date Received
January 14, 1993
Decision Date
June 24, 1994
Product Code
KNG
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
RA
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KNG), ordered by most recent decision date.

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Other Clearances by Huntleigh Healthcare, Inc.

K Number Device Name
K032315 IOP8 INTRA OPERATIVE PROBE
K022786 DVT60
K010744 FLOWTRON UNIVERSAL, MODEL AC600
K012008 STS RANGE , MODELS STS20,STS30,STS40
K002186 VASCULAR ASSIST
K010894 BABY DOPPLEX 3002 (BD3002)
K010889 BABY DOPPLEX 3000 MK 2 (BD3000)
K001882 BABY DOPPLEX 4002-TWINS, MODEL BD4002
K990569 BABY DOPPLEX 4000, MODEL BD 4000
K984307 MODIFICATION OF: RHEO DOPPLEX II
Search all 14 clearances from Huntleigh Healthcare, Inc. →