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

FIRST BEAT/CARDIO BEAT/CALC

K Number: K961116 · Decision Aug 8, 1996
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
19
Review Days
141

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Basic Information

Device Name
FIRST BEAT/CARDIO BEAT/CALC
K Number
K961116
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Medasonics, Inc.
Date Received
March 20, 1996
Decision Date
August 8, 1996
Product Code
IYO
Advisory Committee
Radiology
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
IYO System, Imaging, Pulsed Echo, Ultrasonic

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Other Clearances by Medasonics, Inc.

K Number Device Name
K991441 CADENCE DOPPLER ULTRASOUND SYSTEM
K962796 NEUROGUARD TRANSCRANIAL DOPPLER ULTRASOUND SYSTEM
K914862 CEREBROVASCULAR DIAGNOSTIC SYSTEM; CDS
K911453 OBTRASOUND STETHOSCOPE FETAL CALC
K882018 MEDACORD PVL, PERSONAL VASCULAR LABORATORY
K872292 TRANSPECT TRANSCRANIAL DOPPLER
K854734 MODEL 5320 TED SEQUENTIAL COMP. DE. COMP. LIMB SLE
K833588 VASCULAR LABORATORY TREADMILL VT1
K837481 BF24 DOPPLER MODEL P872 AND P874
K831393 VASCULAB BLOOD PRESSURE CUFF
Search all 19 clearances from Medasonics, Inc. →