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EZEE RETRIEVAL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162059
510(k) Type
Special
Applicant
GENICON, INC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/2016
Days to Decision
65 days
Submission Type
Summary