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OCCLUSION BALLOON CATHETER, MODEL VENOS — Oscor, Inc. (510(k) K081052)

OCCLUSION BALLOON CATHETER, MODEL VENOS — Oscor, Inc. (510(k) K081052) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: OCCLUSION BALLOON CATHETER, MODEL VENOS; Applicant: Oscor, Inc.; Clearance track: 510(k).

Device nameOCCLUSION BALLOON CATHETER, MODEL VENOS
ApplicantOscor, Inc.
Clearance track510(k)
Submission numberK081052
DecisionSubstantially Equivalent
Decision date2008-06-18
Date received2008-04-14
Product codeDYG
Device class2
Medical specialtyCardiovascular
Applicant locationFL, US
SourceopenFDA device

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