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Aeiomed, Inc.

4 FDA 510(k) clearances · Manufacturer

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RecordFirmDate
MODEL 300157 CPAP SYSTEM (K100121)Aeiomed, Inc.2010-07-13
REUSABLE HEADREST WITH NASAL SEAL (K072993)Aeiomed, Inc.2008-02-08
AURA CPAP SYSTEM (K042945)Aeiomed, Inc.2005-03-09
AURA CPAP PATIENT INTERFACE (K042130)Aeiomed, Inc.2004-09-08

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Every clearance here is in the API, with alerts when new ones post.