MODIFICATION OF ACUSON V510B TRANSDUCER

Transducer, Ultrasonic, Diagnostic

ACUSON CORP.

The following data is part of a premarket notification filed by Acuson Corp. with the FDA for Modification Of Acuson V510b Transducer.

Pre-market Notification Details

Device IDK933663
510k NumberK933663
Device Name:MODIFICATION OF ACUSON V510B TRANSDUCER
ClassificationTransducer, Ultrasonic, Diagnostic
Applicant ACUSON CORP. 1220 CHARLESTON RD. Mountain View,  CA  94039 -7393
ContactSheila Pickering
CorrespondentSheila Pickering
ACUSON CORP. 1220 CHARLESTON RD. Mountain View,  CA  94039 -7393
Product CodeITX  
CFR Regulation Number892.1570 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1993-07-28
Decision Date1994-01-21

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