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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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