510(k) K923781

Device
MXR-2000 FLOWMETER
Applicant
PORTER INSTRUMENT CO., INC.
510(k) number
K923781
Product code
CAX  
Decision
Substantially Equivalent (SESE)
Decision date
1993-06-10
Date received
1992-07-28
Regulation
868.2340
Classification name
Flowmeter, Tube, Thorpe, Back-pressure Compensated
Medical specialty
Anesthesiology
Review panel
Anesthesiology
Device class
1
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
& HARTSON
Address
Columbia Sq. 555 Thirteenth St., NW Washington, D.C. DC US 20004 20004

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code CAX  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K910316OHMEDA - LOW FLOW FLOWMETEROhmeda Medical1991-04-12
K884973FR6000 FLOWMETERKey Instruments1989-01-17
K872718SERIES D FLOWMETERPuritan Bennett Corp.1987-08-05
K871452CLASSIC (TM) 200 OXYGEN FLOWMETERThe Timeter Group1987-06-22
K862797AIRCO 2000 SERIES FLOWMETERSAirco, Inc.1986-08-08
K854067SELECT FLOWMETERPrecision Medical, Inc.1985-10-29
K851288OXYGEN DELIVERY MEASURING DEVICEBar-Dix, Inc.1985-09-03
K850559PRESSURE RELIEF ADAPTORPrecision Medical, Inc.1985-04-25
K850560FLOWMETER, BACKPRESSURE COMPENSATED, THORPE TUBEPrecision Medical, Inc.1985-04-17
K834260RECON-2 FLOW CONTROLLERPrecision Metering, Inc.1984-01-10
K812419PRESET FLOWMETERTimeter Instrument Corp.1981-09-21
K812183TIMETER-PRODUCED PURITAN BENNETT AIR ADPTimeter Instrument Corp.1981-08-18
K812128RECON 1Precision Metering, Inc.1981-08-18
K802659RESPIRATORY THERAPY FLOWMETERDesign & Manufacturing Consultants1980-11-12
K802311MO8 OXYGEN FLOWMETERTimeter Instrument Corp.1980-10-23

Legacy Summary#

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FDA Review#

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