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

KC 100 M

K Number: K834285 · Decision Feb 17, 1984
Classifications
1
FEI Numbers
348
Registration Numbers
349
Same Product Code
892
Applicant Total
94
Review Days
94

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Basic Information

Device Name
KC 100 M
K Number
K834285
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1560
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Elscint, Inc.
Date Received
November 15, 1983
Decision Date
February 17, 1984
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 Elscint, Inc.

K Number Device Name
K983313 ADVANCED AUTOMATIC DETECTOR SELECTION OPTION FOR GLORY
K982060 VOLUMAX CT IMAGING SYSTEM
K974344 CT SCOPE
K980306 GYREX 2T PRESTIGE, GYREX PRIMA ITG, GYREX PRIVILEGE, GYREX V-EP
K974614 GYREX 2T PRESTIGE 100-6321-0107, GYREX PRIVILEDGE 100-6326-0102, GYREX PRIMA 1TG 100-6250-0102
K972592 2T PRESTIGE(100-6321-0107)/PRIVILEGE(100-6326-0102)/GYREX V-EP(100-6327-0101)
K970680 GLORY
K965044 GYREX 2T PRESTIGE MODEL NO. 100-6321-0107 AND GYREX PRIVILEGE MODEL NO. 100-6326-0102
K970980 CARDIAC SCORING FOR CT SCANNERS
K970005 GYREX 2T-PRESTIGE
Search all 94 clearances from Elscint, Inc. →