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

MODEL P23XL PHYSIOLOGICAL PRESSURE TRANSDUCER

K Number: K843969 · Decision Jan 23, 1985
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
31
Review Days
104

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Basic Information

Device Name
MODEL P23XL PHYSIOLOGICAL PRESSURE TRANSDUCER
K Number
K843969
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Gould, Inc.
Date Received
October 11, 1984
Decision Date
January 23, 1985
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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K855145 MODEL:TA-ROSE RESONANT OVERSHOOT ELIMINATOR
K854403 MODEL 2120 SPIROSCREEN
K851486 GOULD DISPOSABLE TRANSDUCER & ACCESSORIES-DTX
K850114 C/PES 9201, ECG STRESS TESTING SYS
K850113 C/PES 9103, ECG STRESS TESTING SYSTEM
K843555 CARDIAC COMPUTER SP1445
K843970 MODEL IM1074 END-TIDAL CO2 MODULE
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