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FUJIFILM Endoscope Model EC-760Z-V/L
510(k) Status
Cleared
Active Recalls
None
Manufacturer
Fujifilm Corporation
Country of Origin
—
What it is
Specifications
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Regulatory
FDA 510(k) Clearance
K192664
Cleared 2019-01-01 · Substantially Equivalent
Applicant: Fujifilm Corporation
Reference
Instructions for Use & Documents
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