FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OPUS PACEMAKERS (MODELS 4021, 4033, AND 4034)

K Number: K952363 · Decision Aug 15, 1995
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
3
Applicant Total
43
Review Days
106

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Basic Information

Device Name
OPUS PACEMAKERS (MODELS 4021, 4033, AND 4034)
K Number
K952363
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
872.4565
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ela Medical, Inc.
Date Received
May 1, 1995
Decision Date
August 15, 1995
Product Code
ELA
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

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

Product Code Device Name
ELA Instrument, Hand, Calculus Removal

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (ELA), 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
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. →