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510(k) Data Aggregation
K Number
K011874Device Name
FADASIS MEDICAL FM-1 NO BLENDER
Manufacturer
FADASIS MEDICAL, INC.
Date Cleared
2001-07-20
(35 days)
Product Code
MRO
Regulation Number
868.5165Why did this record match?
Applicant Name (Manufacturer) :
FADASIS MEDICAL, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
The FM-1 NO Blender provides user set concentrations of inhaled Nitric Oxide (NO), in a balance of nitrogen, mixed into a user settable constant flow of oxygen gas that is being delivered to a patient. The intended use for the FM-1 NO Blender is as a back up to a primary nitric oxide delivery system or for short term attended use when a primary delivery device cannot be used. In this capacity, it can be used with a self-inflating manual resuscitator bag. This intended use includes applications within a medical facility. The FM-1 NO blender is not intended for use as a primary NO delivery system for long term use. (Note: These indications for use are unchanged form K003665.
Device Description
The Fadasis Medical FM-1 NO Blender is substantially equivalent to the Fadasis FM-1 NO Blender, The 1 addis Incontaint I 1 1 rith 510(k) premarket notification number K003665. The purpose of this Which was clouded by I DA whan 2000 (EEK, rather than stainless steel, in the capillary tubes.
The new FM-1 NO blender is identical to the predicate FM-1 NO blender with the exception of the capillary tube material, which has been changed to PEEK from stainless steel.
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K Number
K003665Device Name
FADASSI MEDICAL FM-1 NO BLENDER
Manufacturer
FADASIS MEDICAL, INC.
Date Cleared
2001-02-23
(87 days)
Product Code
MRO
Regulation Number
868.5165Why did this record match?
Applicant Name (Manufacturer) :
FADASIS MEDICAL, INC.
AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized
Intended Use
Device Description
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