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

KONTRON SIGMA 1SC DIGITAL ECHOCARDIOGRAPHY SYSTEM

K Number: K862686 · Decision Feb 27, 1987
Classifications
1
FEI Numbers
398
Registration Numbers
399
Same Product Code
408
Applicant Total
57
Review Days
227

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Basic Information

Device Name
KONTRON SIGMA 1SC DIGITAL ECHOCARDIOGRAPHY SYSTEM
K Number
K862686
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1570
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Kontron Instruments, Inc.
Date Received
July 15, 1986
Decision Date
February 27, 1987
Product Code
ITX
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
ITX Transducer, Ultrasonic, Diagnostic

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Other Clearances by Kontron Instruments, Inc.

K Number Device Name
K932268 MODIFICATIONS TO INTRA-AORTIC BALLOONS
K925248 MODIFICATION OF INTRA-AORTIC BALLOON CATHETERS
K923603 INTRA-AORTIC BALLOON PUMP CATHETER - MODIFICATION
K905313 KONTRON INTRA-AORTIC BALLOON PUMP, MODEL KAAT II
K903344 9.5 FR PERCUTANEOUS DB LUMEN 40CC FLEXI-CATH (TM)
K896437 KONTRON SIGMA 44 HVCD ULTRASOUND IMAGING SYSTEM
K892222 9.5F PERCU DOUBLE LUMEN INTRA-AORTIC BALLOON
K882955 SUPERMON NEONATAL NON-INVASIVE BLOOD PRESS. 7283
K896386 MINIMON 7133B PATIENT MONITOR
K896417 KONTRON KOLORMON 7250 PATIENT MONITOR
Search all 57 clearances from Kontron Instruments, Inc. →