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ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K837029
510(k) Type
Traditional
Applicant
AMERICAN ELECTROMEDICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1983
Days to Decision
102 days

ECHOSINE 1000, PULSED A-MODE ULTRASOUND DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K837029
510(k) Type
Traditional
Applicant
AMERICAN ELECTROMEDICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1983
Days to Decision
102 days