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MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861994
510(k) Type
Traditional
Applicant
MEDICOR USA LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1986
Days to Decision
56 days

MODEL RS-3I RADIOGRAPHIC/FLUROSCOPIC X-RAY SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861994
510(k) Type
Traditional
Applicant
MEDICOR USA LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/18/1986
Days to Decision
56 days