ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE— 510(k) K837029
Substantially EquivalentAmerican 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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Data sourced from openFDA. This site is unofficial and independent of the FDA.