FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

PRESSURE WIRE SENSOR, MODELS 12004/12304

K Number: K031662 · Decision Jun 6, 2003
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
62
Applicant Total
24
Review Days
9

Basic Information

Device Name
PRESSURE WIRE SENSOR, MODELS 12004/12304
K Number
K031662
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2870
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
RADI MEDICAL SYSTEMS AB
Date Received
May 28, 2003
Decision Date
June 6, 2003
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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Other Clearances by RADI MEDICAL SYSTEMS AB

K Number Device Name
K123984 QUANTIEN MEASUREMENT SYSTEM
K092105 RADIANALYZER XPRESS
K080813 PRESSUREWIRE CERTUS, CERTUS (300CM), AERIS, AERIS (300CM), RECEIVER
K080206 MODIFICATION TO FEMOSTOP FEMORAL COMPRESSION SYSTEM
K062769 PRESSUREWIRE CERTUS, MODELS 12006 AND 12306
K042628 MODIFICATION TO: RADIANALYZER, MODEL 12711
K033291 TOPSEAL HEMOSTATIC DRESSING, MODEL 11150
K024107 FEMOSTOP FEMORAL COMPRESSION SYSTEM
K022188 RADIANALYZER, MODEL 12710
K022187 PRESSURE WIRE SENSOR, MODELS 12003/12303, 12004/12304
Search all 24 clearances from RADI MEDICAL SYSTEMS AB →