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ZEN-2090 PRO, FLUOROSCOPIC X-RAY SYSTEM, MODEL ZEN-2090 PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091918
510(k) Type
Traditional
Applicant
Genoray Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2009
Days to Decision
99 days
Submission Type
Summary

ZEN-2090 PRO, FLUOROSCOPIC X-RAY SYSTEM, MODEL ZEN-2090 PRO

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091918
510(k) Type
Traditional
Applicant
Genoray Co., Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/7/2009
Days to Decision
99 days
Submission Type
Summary