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

ELATEC HOLTER ANALYZER

K Number: K895806 · Decision Apr 4, 1990
Classifications
1
FEI Numbers
121
Registration Numbers
121
Same Product Code
397
Applicant Total
43
Review Days
188

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Basic Information

Device Name
ELATEC HOLTER ANALYZER
K Number
K895806
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1025
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ela Medical, Inc.
Date Received
September 28, 1989
Decision Date
April 4, 1990
Product Code
DSI
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
DSI Detector And Alarm, Arrhythmia

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Other Clearances by Ela Medical, Inc.

K Number Device Name
K042002 SYNESCOPE, EASYSCOPE, SYNECOM, HOLTERREADER
K032466 SPIDERVIEW
K002817 SYNETEC
K993448 STELA UT46 AND BT45/46 STRAIGHT TINED PACING LEADS, STELA UJ45 AND BJ44/45 J-SHAPED TINED PACING LEADS
K000029 STELA UT46 AND BT45/46 STRAIGHT TINED PACING LEADS, STELA UJ45 AND BJ44/45 J-SHAPED TINED PACING LEADS
K990727 SYNEFLASH & SYNEVIEW
K972574 STELA MODEL UJ45 PACING LEADS
K970072 OPUS S MODEL 4121 AND 4124 PACEMAKERS
K963738 STELA MODEL BJ44 AND BJ45 PACING LEADS
K952364 OPUS PACEMAKERS (MODELS 4001, 4003, 4004, 4023, 4024)
Search all 43 clearances from Ela Medical, Inc. →