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COXEL FLINGER 2500/5000 3-D IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912410
510(k) Type
Traditional
Applicant
REALITY IMAGING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/13/1991
Days to Decision
74 days
Submission Type
Statement