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

NMI Port, NMI Port II

K Number: K153228 · Decision Dec 4, 2015
Classifications
1
FEI Numbers
57
Registration Numbers
57
Same Product Code
287
Applicant Total
35
Review Days
28

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Basic Information

Device Name
NMI Port, NMI Port II
K Number
K153228
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
880.5965
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Navilyst Medical, Inc.
Date Received
November 6, 2015
Decision Date
December 4, 2015
Product Code
LJT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

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K150407 BioFlo Midline Catheter
K150527 Xcela Power Injectable PICC
K150448 NMI PICC III and NMI PICC IV
K142616 PICC Maximal Barrier Nursing Kit
K140194 NAMIC RCS SYRINGE
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