FDA 510(k) FDA class 3 Substantially Equivalent - Subject to Tracking Reg. 🇺🇸 United States

STELA MODEL UJ45 PACING LEADS

K Number: K972574 · Decision Jan 8, 1998
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
43
Review Days
182

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Basic Information

Device Name
STELA MODEL UJ45 PACING LEADS
K Number
K972574
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent - Subject to Tracking Reg.
Applicant
Ela Medical, Inc.
Date Received
July 10, 1997
Decision Date
January 8, 1998
Product Code
DTB
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
DTB Permanent Pacemaker Electrode

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DTB), ordered by most recent decision date.

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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
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 43 clearances from Ela Medical, Inc. →