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G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902984
510(k) Type
Traditional
Applicant
ELECTROMEK DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1990
Days to Decision
122 days

G.E. AMX 110, AMX II AND AMX 3 X-RAY UNITS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902984
510(k) Type
Traditional
Applicant
ELECTROMEK DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1990
Days to Decision
122 days