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Results for “KSEA NEURO-FIBERSCOPE”
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Ksea Neuro-Fiberscope
Open recall
Karl Storz Endoscopy-America, Inc.
·
,
FDA registration: United States
Group of variants
FDA 510(k)
K002788
Active
Cleared 23 Oct 2000
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
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