MARINR SERIES EP DIAGNOSTI CATHETERS

Catheter, Electrode Recording, Or Probe, Electrode Recording

MEDTRONIC CARDIORHYTHM

The following data is part of a premarket notification filed by Medtronic Cardiorhythm with the FDA for Marinr Series Ep Diagnosti Catheters.

Pre-market Notification Details

Device IDK951347
510k NumberK951347
Device Name:MARINR SERIES EP DIAGNOSTI CATHETERS
ClassificationCatheter, Electrode Recording, Or Probe, Electrode Recording
Applicant MEDTRONIC CARDIORHYTHM 130 RIO ROBLES San Jose,  CA  95134 -1806
ContactCraig J Coombs
CorrespondentCraig J Coombs
MEDTRONIC CARDIORHYTHM 130 RIO ROBLES San Jose,  CA  95134 -1806
Product CodeDRF  
CFR Regulation Number870.1220 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1995-02-28
Decision Date1995-05-10

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
00613994947543 K951347 000
00613994947222 K951347 000
00613994947215 K951347 000
00613994947208 K951347 000
00613994947192 K951347 000

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