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

INFUSET W/HUBER NEEDLE

K Number: K844313 · Decision Jan 22, 1985
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
22
Review Days
77

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Basic Information

Device Name
INFUSET W/HUBER NEEDLE
K Number
K844313
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Med Fusion Systems, Inc.
Date Received
November 6, 1984
Decision Date
January 22, 1985
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

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K864407 REFILLABLE SYRINGE
K863814 BAG SPIKE EXTENSION SET
K860616 VOLUME CONTROL SET WITH EXTENSION
K860803 IV FILTER EXTENSION SET
K842984 EXTENSION SET W/INJECTION SITE
K842143 BENT WINGED MINI-VOL INFUSION SET
K841882 THREE WAY INFUSION SET
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