Drakon And Sequre Microcatheters

Catheter, Intravascular, Diagnostic

Accurate Medical Therapeutics Ltd

The following data is part of a premarket notification filed by Accurate Medical Therapeutics Ltd with the FDA for Drakon And Sequre Microcatheters.

Pre-market Notification Details

Device IDK203487
510k NumberK203487
Device Name:Drakon And Sequre Microcatheters
ClassificationCatheter, Intravascular, Diagnostic
Applicant Accurate Medical Therapeutics Ltd 19 Eli Hurvitz Street Rehovot,  IL 7608802
ContactOsnat Harbater
CorrespondentOsnat Harbater
Accurate Medical Therapeutics Ltd 19 Eli Hurvitz Street Rehovot,  IL 7608802
Product CodeDQO  
CFR Regulation Number870.1200 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeSpecial
3rd Party ReviewedNo
Combination ProductNo
Date Received2020-11-27
Decision Date2020-12-11

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
07290017268378 K203487 000
07290017268361 K203487 000

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