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

VOLUME COMPUTATION SOFTWARE PACKAGE

K Number: K890638 · Decision Aug 7, 1989
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
71
Applicant Total
94
Review Days
180

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Basic Information

Device Name
VOLUME COMPUTATION SOFTWARE PACKAGE
K Number
K890638
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2880
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Elscint, Inc.
Date Received
February 8, 1989
Decision Date
August 7, 1989
Product Code
JOP
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JOP Transducer, Ultrasonic

Similar 510(k) Clearances

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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. →