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

SENTORR ARTERIAL PRESSURE SENSOR

K Number: K880830 · Decision Aug 12, 1988
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
63
Applicant Total
120
Review Days
164

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Basic Information

Device Name
SENTORR ARTERIAL PRESSURE SENSOR
K Number
K880830
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Ohmeda Medical
Date Received
March 1, 1988
Decision Date
August 12, 1988
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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K070377 GIRAFFE AND PANDA WARMER
K070210 GIRAFFE AND PANDA T- PIECE RESUSCITATION SYSTEM
K070247 GIRAFFE AND PANDA BAG AND MASK RESUSCITATION SYSTEM
K040068 BILIBLANKET PLUS HIGH OUTPUT PHOTOTHERAPY SYSTEM
K020543 OHMEDA MEDICAL GIRAFFE OMNIBED
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