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

SONOTRAX ULTRASONIC FETAL AND VASCULAR POCKET DOPPLER, MODELS LITE, BASIC, PRO, II, II PRO AND VASCULAR

K Number: K080087 · Decision Mar 11, 2008
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
59
Applicant Total
92
Review Days
60

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Basic Information

Device Name
SONOTRAX ULTRASONIC FETAL AND VASCULAR POCKET DOPPLER, MODELS LITE, BASIC, PRO, II, II PRO AND VASCULAR
K Number
K080087
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.2660
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Edan Instruments, Inc.
Date Received
January 11, 2008
Decision Date
March 11, 2008
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

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Other Clearances by Edan Instruments, Inc.

K Number Device Name
K251591 Holter ECG and ABP system (HolterABP)
K251268 Diagnostic Ultrasound System (Nano C5, Nano C5 EXP, Nano L12, and Nano L12 EXP)
K241882 Fetal & Maternal Monitor (F15A, F15A Air)
K250179 Patient Monitor (CX10, CX12, CX15, UX10, UX12, UX15)
K250214 Acclarix AX8 Series Diagnostic Ultrasound System (Model: Acclarix AX7, Acclarix AX8, Acclarix AX75, Acclarix AX78, Acclarix AX8 Exp, Acclarix AX8 Super), Acclarix AX9 Series Diagnostic Ultrasound Szystem (Model: Acclarix AX9 Basic, Acclarix AX9, Acclarix AX9 Exp, Acclarix AX9 Super, Acclarix AX85, Acclarix AX88)
K240320 Patient Monitor (RespArray)
K232786 Stimulation System (PA series, PR series, S series and Q series)
K232962 Patient Monitor (iX10, iX12, iX15)
K233038 Vital Signs monitor, Model: iM3s, iM3As, iM3Bs, iHM3s
K232694 Central Monitoring System (MFM-CMS)
Search all 92 clearances from Edan Instruments, Inc. →