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DiLumen Endolumenal Interventional Platform
510(k) Status
Cleared
Active Recalls
None
Manufacturer
Lumendi, LLC
Country of Origin
—
What it is
Specifications
No specifications on file yet. The manufacturer hasn't published spec data — claim this listing to add it.
Regulatory
FDA 510(k) Clearance
K162428
Cleared 2016-01-02 · Substantially Equivalent
Applicant: Lumendi, LLC
Reference
Instructions for Use & Documents
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Education & How-to
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