FDA 510(k) Unknown 🇺🇸 United States

MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN

K Number: K842342 · Decision Jun 14, 1984
Classifications
0
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
11
Review Days

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Basic Information

Device Name
MWI 888 & 666 DOUBLE LUMEN SUBCLAVIAN
K Number
K842342
Clearance Type
Traditional
Decision
Unknown
Applicant
Med-West, Inc.
Date Received
June 14, 1984
Decision Date
June 14, 1984
Advisory Committee
Unknown
Review Advisory Committee
GU
Third Party
N

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K852162 MNI 400 INJECTION CAPS
K832124 CPC, COUBLE LUMEN CARDIOPLEGIA-AIR ASPI
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K831401 SINGLE NEEDLE SUBCLAVIAN VEIN ACCESS
K831440 SINGLE NEEDLE SUBCLAVIAN VEIN MWI250/260
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