ALGO 7i

Stimulator, Auditory, Evoked Response

Path Medical GmbH

The following data is part of a premarket notification filed by Path Medical Gmbh with the FDA for Algo 7i.

Pre-market Notification Details

Device IDK211147
510k NumberK211147
Device Name:ALGO 7i
ClassificationStimulator, Auditory, Evoked Response
Applicant Path Medical GmbH Landsberger Strasse 65 Germering,  DE 82110
ContactIng. Johann Oswald
CorrespondentIng. Johann Oswald
Path Medical GmbH Landsberger Strasse 65 Germering,  DE 82110
Product CodeGWJ  
CFR Regulation Number882.1900 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received2021-04-19
Decision Date2021-10-14

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
04260223145490 K211147 000
04260223145483 K211147 000
04260223145476 K211147 000
04260223145469 K211147 000
04260223145421 K211147 000
04260223145414 K211147 000

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