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FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141743
510(k) Type
Traditional
Applicant
RADIOLOGY SOLUTIONS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2014
Days to Decision
95 days
Submission Type
Summary

FUSION DIGITAL DIAGNOSTIC X-RAY UPGRADE KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K141743
510(k) Type
Traditional
Applicant
RADIOLOGY SOLUTIONS LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/3/2014
Days to Decision
95 days
Submission Type
Summary