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

ECG MODULE

K Number: K862553 · Decision Nov 7, 1986
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
94
Review Days
127

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Basic Information

Device Name
ECG MODULE
K Number
K862553
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Elscint, Inc.
Date Received
July 3, 1986
Decision Date
November 7, 1986
Product Code
DPS
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
DPS Electrocardiograph

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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. →