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

MEDTRONIC INTRAVASCULAR BLOOD GAS MONITORING

K Number: K891013 · Decision Aug 2, 1989
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
14
Applicant Total
475
Review Days
155

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Basic Information

Device Name
MEDTRONIC INTRAVASCULAR BLOOD GAS MONITORING
K Number
K891013
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.1150
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Medtronic Vascular
Date Received
February 28, 1989
Decision Date
August 2, 1989
Product Code
CCC
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CCC Analyzer, Gas, Carbon-Dioxide, Partial Pressure, Blood-Phase, Indwelling

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K Number Device Name
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K232190 6F Sherpa NX Balanced Guide Catheter, 7F Sherpa NX Balanced Guide Catheter
K230156 5F Launcher Guide Catheter, 6F Launcher Guide Catheter, 7F Launcher Guide Catheter, 8F Launcher Guide Catheter
K220773 Everest 20 Inflation Device and 3-way Stopcock (AC2200);Everest 30 Inflation Device and 3-way Stopcock (AC3200);Everest 20 Survival Kit containing:1. Everest 20 Device with 3-way Stopcock, 2. Piton Y-Adaptor ,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC2205P); Everest 30 Survival Kit containing:1. Everest 30 Device with 3-way Stopcock, 2. Piton Y-Adaptor,3. Metal Guidewire Insertion Needle, 4. Torque Handle (AC3205P)
K192296 Medtronic 6F Taiga Guiding Catheter
K173515 Admiral Xtreme
K162097 InTRAkit
K162027 TRAcelet Compression Device
K161287 DxTerity, DxTerity TRA, DxTerity Angio-Kit, DxTerity EZ-Pak, DxTerity TRA Angio-Kit, DxTerity TRA EZ-Pak
K133539 TOTAL ACROSS
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