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

SUSI II PACEMAKER SURVEILLANCE MONITOR

K Number: K792602 · Decision Mar 25, 1980
Classifications
1
FEI Numbers
6
Registration Numbers
6
Same Product Code
29
Applicant Total
42
Review Days
98

Basic Information

Device Name
SUSI II PACEMAKER SURVEILLANCE MONITOR
K Number
K792602
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3630
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
ELA MEDICAL, INC.
Date Received
December 18, 1979
Decision Date
March 25, 1980
Product Code
DTC
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
DTC Analyzer, Pacemaker Generator Function

Similar 510(k) Clearances

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Other Clearances by ELA MEDICAL, INC.

K Number Device Name
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)
K952363 OPUS PACEMAKERS (MODELS 4021, 4033, AND 4034)
Search all 42 clearances from ELA MEDICAL, INC. →