Last synced on 25 January 2026 at 3:41 am

SSD-203 ULTRASONIC SCANNER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813398
510(k) Type
Traditional
Applicant
U. S. A. IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1982
Days to Decision
87 days

SSD-203 ULTRASONIC SCANNER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K813398
510(k) Type
Traditional
Applicant
U. S. A. IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/1982
Days to Decision
87 days