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

LifeGlobal Micro Tips

K Number: K152581 · Decision Apr 11, 2016
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
25
Applicant Total
3
Review Days
214

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Basic Information

Device Name
LifeGlobal Micro Tips
K Number
K152581
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6130
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life Global Group, LLC
Date Received
September 10, 2015
Decision Date
April 11, 2016
Product Code
MQH
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
MQH Microtools, Assisted Reproduction (Pipettes)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MQH), ordered by most recent decision date.

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Other Clearances by Life Global Group, LLC

K Number Device Name
K142991 LifeGlobal Global Total w/HSA, LifeGlobal Global Total for Fertilization w/HSA, LifeGlobal Global Total w/HEPES W/HSA
K143498 LifeGlobal Global HP