DeviceClearance

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
Download summary PDFView on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.