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

MINATURE PRESSURE TRANSDUCER

K Number: K834040 · Decision Feb 10, 1984
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
22
Review Days
79

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Basic Information

Device Name
MINATURE PRESSURE TRANSDUCER
K Number
K834040
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Carbomedics, Inc.
Date Received
November 23, 1983
Decision Date
February 10, 1984
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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K960169 CARBOMEDICS VALVE TESTER
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K952184 CARBOMEDICS SUPRA-ANNULAR VALVE SIZER
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