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

VACUETTE SAFELINK Holder with male luer lock

K Number: K180545 · Decision May 21, 2018
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
5
Review Days
81

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Basic Information

Device Name
VACUETTE SAFELINK Holder with male luer lock
K Number
K180545
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Greiner Bio-One Na, Inc.
Date Received
March 1, 2018
Decision Date
May 21, 2018
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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K Number Device Name
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K163436 Greiner Vacuette Urine Count and Culture, Mannitol tube
K160532 Greiner Holdex