SSA-770A, APLIO VERSION 5.5

System, Imaging, Pulsed Doppler, Ultrasonic

TOSHIBA MEDICAL SYSTEMS CORPORATION

The following data is part of a premarket notification filed by Toshiba Medical Systems Corporation with the FDA for Ssa-770a, Aplio Version 5.5.

Pre-market Notification Details

Device IDK041499
510k NumberK041499
Device Name:SSA-770A, APLIO VERSION 5.5
ClassificationSystem, Imaging, Pulsed Doppler, Ultrasonic
Applicant TOSHIBA MEDICAL SYSTEMS CORPORATION 2441 MICHELLE DRIVE Tustin,  CA  92780
ContactPaul Biggins
CorrespondentMark Job
REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul,  MN  55114
Product CodeIYN  
Subsequent Product CodeITX
Subsequent Product CodeIYO
CFR Regulation Number892.1550 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedYes
Combination ProductNo
Date Received2004-06-07
Decision Date2004-06-10
Summary:summary

NIH GUDID Devices

Device IdentifiersubmissionNumberSupplement
04987670001802 K041499 000
04987670001284 K041499 000
04987670001277 K041499 000
04987670001246 K041499 000
04987670000942 K041499 000
04987670000911 K041499 000

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