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510(k) Data Aggregation
K Number
K001121Device Name
OXYGEN APPLIED SYMPTOM IMPROVEMENT SYSTEM (OASIS)
Manufacturer
ENGINEERED MEDICAL TECHNOLOGY, INC.
Date Cleared
2001-11-29
(601 days)
Product Code
CBF
Regulation Number
868.5470Why did this record match?
Applicant Name (Manufacturer) :
ENGINEERED MEDICAL TECHNOLOGY, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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