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G.E. POLARIX II C-ARM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902982
510(k) Type
Traditional
Applicant
ELECTROMEK DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1990
Days to Decision
140 days

G.E. POLARIX II C-ARM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K902982
510(k) Type
Traditional
Applicant
ELECTROMEK DIAGNOSTIC SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/1990
Days to Decision
140 days