FDA 510(k) Applications Submitted by ATL ULTRASOUND, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K994373 12/27/1999 HDI 1500/SA 8800 ULTRASOUND SYSTEM WITH MULTIPLANE TRANSESOPHAGEAL ULTRASOUND TRANSDUCER (MTP7-4) ATL ULTRASOUND, INC.
K002003 06/30/2000 HDI 5000 ULTRASOUND SYSTEM WITH EXTENDED FIELD OF VIEW IMAGING ATL ULTRASOUND, INC.


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