FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DISPOSABLE CATHETER PRESSURE TRANSDUCER

K Number: K894033 · Decision Oct 17, 1989
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
20
Review Days
133

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Basic Information

Device Name
DISPOSABLE CATHETER PRESSURE TRANSDUCER
K Number
K894033
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Deseret Medical, Inc.
Date Received
June 6, 1989
Decision Date
October 17, 1989
Product Code
DXO
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXO Transducer, Pressure, Catheter Tip

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K Number Device Name
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K904122 INSYTE-A ARTERIAL CATHETERIZATION UNIT
K900116 DESERET OPTIMA INTRAVASCULAR CATHETER
K895735 DESERET MULTILUMEN SUBCLAVIAN CATHETER
K895734 DESERET INTRAVASCULAR CATHETER
K893406 DESERET PRN ADAPTER
K882797 LUER-LOK MULTIFLO ADAPTER
K882798 MULTIFLO ADAPTER
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