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

Additive Cap

K Number: K190305 · Decision Apr 30, 2019
Classifications
1
FEI Numbers
86
Registration Numbers
86
Same Product Code
116
Applicant Total
7
Review Days
77

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Basic Information

Device Name
Additive Cap
K Number
K190305
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
International Medical Industries, Inc.
Date Received
February 12, 2019
Decision Date
April 30, 2019
Product Code
KPE
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
KPE Container, I.V.

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