DIASONICS DLA-100

System, Imaging, Pulsed Echo, Ultrasonic

DIASONICS, INC.

The following data is part of a premarket notification filed by Diasonics, Inc. with the FDA for Diasonics Dla-100.

Pre-market Notification Details

Device IDK833667
510k NumberK833667
Device Name:DIASONICS DLA-100
ClassificationSystem, Imaging, Pulsed Echo, Ultrasonic
Applicant DIASONICS, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeIYO  
CFR Regulation Number892.1560 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1983-10-19
Decision Date1984-05-09

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