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

UNI-PICC

K Number: K130034 · Decision Mar 8, 2013
Classifications
1
FEI Numbers
90
Registration Numbers
90
Same Product Code
301
Applicant Total
11
Review Days
60

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Basic Information

Device Name
UNI-PICC
K Number
K130034
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5970
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Health Line International Corporation
Date Received
January 7, 2013
Decision Date
March 8, 2013
Product Code
LJS
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
LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days

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