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KIPPMED I.V. MANIFOLD — The Kipp Group (510(k) K000152)

KIPPMED I.V. MANIFOLD — The Kipp Group (510(k) K000152) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: KIPPMED I.V. MANIFOLD; Applicant: The Kipp Group; Clearance track: 510(k).

Device nameKIPPMED I.V. MANIFOLD
ApplicantThe Kipp Group
Clearance track510(k)
Submission numberK000152
DecisionSubstantially Equivalent
Decision date2000-02-29
Date received2000-01-19
Product codeFPA
Device class2
Medical specialtyGeneral Hospital
Applicant locationCA, US
SourceopenFDA device

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