ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE— 510(k) K837029

Substantially Equivalent

American Electromedics Corp.

FDA 510(k) clearance K837029 for ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE, Substantially Equivalent on 1983-03-22. Applicant: American Electromedics Corp..

Clearance details

Applicant
American Electromedics Corp.
Advisory panel
Unknown
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Hudson, NH, US
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