CALPREST

Calprotectin, Fecal

EUROSPITAL S.P.A.

The following data is part of a premarket notification filed by Eurospital S.p.a. with the FDA for Calprest.

Pre-market Notification Details

Device IDK130945
510k NumberK130945
Device Name:CALPREST
ClassificationCalprotectin, Fecal
Applicant EUROSPITAL S.P.A. 3331 EAGLE WATCH DRIVE Woodstock,  GA  30189
ContactDavid Dunn
CorrespondentDavid Dunn
EUROSPITAL S.P.A. 3331 EAGLE WATCH DRIVE Woodstock,  GA  30189
Product CodeNXO  
CFR Regulation Number866.5180 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2013-04-04
Decision Date2014-01-16
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
08028169204093 K130945 000

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